Allele Registry

Canonical Allele Identifier: PA2828490168

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV001950093

RCV002479473

ClinVar Variation:

1429458

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358382.1:p.Arg18Gln	CA322292 NM_001371453.1:c.53G>A