别名

RS396991,V158F
Allele Registry ID:CA1211378
ClinVar ID:

突变位点

Ref. Build: GRCh37   Ensembl Version: 75
Chr.StartStopRef. sVar. Bases
1161514542161514542AC
Transcript
ENST00000367969.3

基因序列

NC_000001.10:g.161514542A>003eC