Allele Registry

Canonical Allele Identifier: PA2828487786

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000196315

ClinVar Variation:

214167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358372.1:p.Arg185Trp	CA320735 NM_001371443.1:c.553C>T