Canonical Allele Identifier: PA2828473158
Gene: BCS1L HGNC NCBI

Linked Data

ClinVar Variation Id: 6166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361014.1:p.Val353Met
CA117999
NM_001374085.1:c.1057G>A