Allele Registry

Canonical Allele Identifier: PA2826153394

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV001324880

ClinVar Variation:

1024666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171944.1:p.Glu218Gly	CA66761115 NM_001185015.2:c.653A>G