Allele Registry

Canonical Allele Identifier: PA2828761433

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV001324880

ClinVar Variation:

1024666

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365376.1:p.Glu212Gly	CA66761115 NM_001378447.1:c.635A>G