VHL L89P (c.266T>003eC)


别名

C.266T>003eC,LEU89PRO,RS5030807
Allele Registry ID:CA020207
ClinVar ID:182979

突变位点

Ref. Build: GRCh37   Ensembl Version: 75
Chr.StartStopRef. sVar. Bases
31018379710183797TC
Transcript
ENST0000

基因序列

NM_000551.3:c.266T>003eC
NP_000542.1:p.Leu89Pro
NC_000003.11:g.10183797T>003eC
ENST00000256474.2:c.266T>003eC