Allele Registry

Canonical Allele Identifier: PA2828487875

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000114392

ClinVar Variation:

126497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358372.1:p.Tyr301Asn	CA151154 NM_001371443.1:c.901T>A