Allele Registry

Canonical Allele Identifier: PA1139744670

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV000264680

RCV000455477

ClinVar Variation:

334917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365375.1:p.Ala134Val	CA2154843 NM_001378446.1:c.401C>T