别名

RS1801133,C677T,ALA222VAL
Allele Registry ID:CA170990
ClinVar ID:3520

突变位点

Ref. Build: GRCh37   Ensembl Version: 75
Chr.StartStopRef. sVar. Bases
11185637811856378GA
Transcript
ENST00000376592.1

基因序列

NM_005957.4:c.665C>003eT
NP_005948.3:p.Ala222Val
ENST00000376592.1:c.665G>003eA
NC_000001.10:g.11856378G>003eA