Canonical Allele Identifier: PA2828488925
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 1302936
ClinVar RCV Id: RCV001756435 RCV002496067
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358377.1:p.Arg69His
CA2109622
NM_001371448.1:c.206G>A