Canonical Allele Identifier: PA2580219861
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 2229599
ClinVar RCV Id: RCV002697567
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358380.1:p.Ala34Asp
CA350626850
NM_001371451.1:c.101C>A