Allele Registry

Canonical Allele Identifier: PA2828490457

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000049827

ClinVar Variation:

56414

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358383.1:p.Val160Ala	CA144350 NM_001371454.1:c.479T>C