Allele Registry

Canonical Allele Identifier: PA2580346264

Gene: SCN10A HGNC NCBI

ClinVar RCV:

RCV002373137

ClinVar Variation:

1736118

HGVS (amino-acid)	Matching Registered Transcripts
NP_006505.4:p.Ala1304Ser	CA2320072 NM_006514.4:c.3910G>T