Allele Registry

Canonical Allele Identifier: PA2826833427

Gene: SCN10A HGNC NCBI

ClinVar RCV:

RCV000466946

RCV000613459

RCV000987249

RCV002254167

RCV002341091

RCV002496819

RCV003431025

ClinVar Variation:

414633

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280235.2:p.Gly1661Ser	CA2319765 NM_001293306.2:c.4981G>A