Allele Registry

Canonical Allele Identifier: PA2829527586

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV000264680

RCV000455477

ClinVar Variation:

334917

HGVS (amino-acid)	Matching Registered Transcripts
NP_004501.4:p.Ala128Val	CA2154843 NM_004510.4:c.383C>T