Allele Registry

Canonical Allele Identifier: PA2827021460

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000049827

ClinVar Variation:

56414

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305765.1:p.Val207Ala	CA144350 NM_001318836.2:c.620T>C