Allele Registry

Canonical Allele Identifier: PA1139743096

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000196315

ClinVar Variation:

214167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358380.1:p.Arg65Trp	CA320735 NM_001371451.1:c.193C>T