Allele Registry

Canonical Allele Identifier: PA916024063

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006540

ClinVar Variation:

6165

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305765.1:p.Arg35Pro	CA117994 NM_001318836.2:c.104G>C