Allele Registry

Canonical Allele Identifier: PA2828180001

Gene: SCN9A HGNC NCBI

ClinVar Allele:

21407

ClinVar RCV:

RCV000006740

RCV000215091

RCV000555200

RCV000765531

RCV002408455

RCV004525845

ClinVar Variation:

6368

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile62Val	CA118170 NM_001365536.1:c.184A>G