Allele Registry

Canonical Allele Identifier: PA2828489216

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006549

ClinVar Variation:

6173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001358378.1:p.Thr50Ala	CA118036 NM_001371449.1:c.148A>G