Allele Registry

Canonical Allele Identifier: PA2573211207

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV002015958

ClinVar Variation:

1500840

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Val1310Ile	CA349064811 NM_001365536.1:c.3928G>A