Canonical Allele Identifier: PA2825459205
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2229599
ClinVar RCV Id: RCV002697567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001073335.1:p.Ala154Asp
CA350626850
NM_001079866.2:c.461C>A