Allele Registry

Canonical Allele Identifier: PA2829527661

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV001324880

ClinVar Variation:

1024666

HGVS (amino-acid)	Matching Registered Transcripts
NP_004501.4:p.Glu212Gly	CA66761115 NM_004510.4:c.635A>G