Allele Registry

Canonical Allele Identifier: PA2828490720

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000200623

RCV000714568

RCV000949252

RCV001137961

RCV001137962

RCV001137963

ClinVar Variation:

214159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358385.1:p.Val38Ile	CA325212 NM_001371456.1:c.112G>A