Canonical Allele Identifier: PA2826439912
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2041499
ClinVar RCV Id: RCV002903015
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244271.1:p.Arg73Gly
CA65808578
NM_001257342.2:c.217C>G