Canonical Allele Identifier: PA2828490300
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358382.1:p.Val186Met
CA117999
NM_001371453.1:c.556G>A