Allele Registry

Canonical Allele Identifier: PA2828490167

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000196315

ClinVar Variation:

214167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358382.1:p.Arg18Trp	CA320735 NM_001371453.1:c.52C>T