Allele Registry

Canonical Allele Identifier: PA2828489459

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006541

RCV001851699

RCV003472986

ClinVar Variation:

6166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358378.1:p.Val353Met	CA117999 NM_001371449.1:c.1057G>A