Allele Registry

Canonical Allele Identifier: PA1139743088

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000049826

ClinVar Variation:

56413

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358380.1:p.Arg24Gln	CA144345 NM_001371451.1:c.71G>A