Allele Registry

Canonical Allele Identifier: PA916018829

Gene: SCN10A HGNC NCBI

ClinVar RCV:

RCV000253983

RCV001510995

RCV001807173

RCV002321930

ClinVar Variation:

259997

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280236.2:p.Leu994Pro	CA2320282 NM_001293307.2:c.2981T>C