Allele Registry

Canonical Allele Identifier: PA2827054527

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV003542635

ClinVar Variation:

2692639

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307646.1:p.Arg45Gly	CA2109609 NM_001320717.2:c.133C>G