Canonical Allele Identifier: PA2826440034
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 381524
ClinVar RCV Id: RCV000432529 RCV001329213 RCV002285017
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244271.1:p.Gly129Arg
CA16604118
NM_001257342.2:c.385G>A
CA350626484
NM_001257342.2:c.385G>C