Allele Registry

Canonical Allele Identifier: PA118039

Gene: BCS1L HGNC NCBI

ClinVar RCV:

RCV000006549

ClinVar Variation:

6173

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244273.1:p.Thr50Ala	CA118036 NM_001257344.2:c.148A>G