Allele Registry

Canonical Allele Identifier: PA2828487999

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000197059

RCV000415034

RCV000623904

RCV000675122

RCV001810436

RCV003474948

ClinVar Variation:

214160

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358373.1:p.Arg69Cys	CA321501 NM_001371444.1:c.205C>T