Allele Registry

Canonical Allele Identifier: PA324388

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000199842

RCV003226245

RCV003474949

ClinVar Variation:

214166

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244273.1:p.Arg109Trp	CA324385 NM_001257344.2:c.325C>T