Canonical Allele Identifier: PA2828489281
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 381524
ClinVar RCV Id: RCV000432529 RCV001329213 RCV002285017
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358378.1:p.Gly129Arg
CA16604118
NM_001371449.1:c.385G>A
CA350626484
NM_001371449.1:c.385G>C