Allele Registry

Canonical Allele Identifier: PA2741911659

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV003542635

ClinVar Variation:

2692639

HGVS (amino-acid)	Matching Registered Transcripts
NP_004319.1:p.Arg45Gly	CA2109609 NM_004328.5:c.133C>G