Allele Registry

Canonical Allele Identifier: PA2826833148

Gene: SCN10A HGNC NCBI

ClinVar RCV:

RCV002373137

ClinVar Variation:

1736118

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280235.2:p.Ala1303Ser	CA2320072 NM_001293306.2:c.3907G>T