Allele Registry

Canonical Allele Identifier: PA916045389

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006731

RCV000691966

RCV001090456

ClinVar Variation:

6359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Val1310Phe	CA118149 NM_001365536.1:c.3928G>T