Allele Registry

Canonical Allele Identifier: PA2828761393

Gene: SP110 HGNC NCBI

ClinVar RCV:

RCV000264680

RCV000455477

ClinVar Variation:

334917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365376.1:p.Ala128Val	CA2154843 NM_001378447.1:c.383C>T