Allele Registry

Canonical Allele Identifier: PA2826834587

Gene: SCN10A HGNC NCBI

ClinVar RCV:

RCV002373137

ClinVar Variation:

1736118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280236.2:p.Ala1206Ser	CA2320072 NM_001293307.2:c.3616G>T