Allele Registry

Canonical Allele Identifier: PA2828489537

Gene: BCS1L HGNC NCBI

ClinVar Variation Id: 1120065

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358379.1:p.Ser65Arg	CA2109617 NM_001371450.1:c.193A>C CA350625828 NM_001371450.1:c.195C>A CA350625829 NM_001371450.1:c.195C>G