Canonical Allele Identifier: PA2828490478
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6166
ClinVar RCV Id: RCV000006541 RCV001851699 RCV003472986
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358383.1:p.Val186Met
CA117999
NM_001371454.1:c.556G>A