Allele Registry

Canonical Allele Identifier: PA2827021353

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV001950093

RCV002479473

ClinVar Variation:

1429458

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305765.1:p.Arg65Gln	CA322292 NM_001318836.2:c.194G>A