Allele Registry

Canonical Allele Identifier: PA916045388

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006729

ClinVar Variation:

6357

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Val1309Asp	CA118143 NM_001365536.1:c.3926T>A