Allele Registry

Canonical Allele Identifier: PA2828490636

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000049827

ClinVar Variation:

56414

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358384.1:p.Val160Ala	CA144350 NM_001371455.1:c.479T>C