Allele Registry

Canonical Allele Identifier: PA2499255972

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV001324880

ClinVar Variation:

1024666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365375.1:p.Glu218Gly	CA66761115 NM_001378446.1:c.653A>G