Allele Registry

Canonical Allele Identifier: PA118035

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006548

ClinVar Variation:

6172

HGVS (amino-acid)	Matching Registered Transcripts
NP_004319.1:p.Gly35Arg	CA118031 NM_004328.5:c.103G>C