VHL S168T (c.503G>003eC)


别名

C.503G>003eC,SER168THR
Allele Registry ID:CA351756183
ClinVar ID:

突变位点

Ref. Build: GRCh37   Ensembl Version: 75
Chr.StartStopRef. sVar. Bases
31019151010191510GC
Transcript
ENST

基因序列

ENST00000256474.2:c.503G>003eC
NC_000003.11:g.10191510G>003eC
NM_000551.3:c.503G>003eC
NP_000542.1:p.Ser168Thr