Allele Registry

Canonical Allele Identifier: PA916045420

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006732

RCV002512850

ClinVar Variation:

6360

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile1472Thr	CA118152 NM_001365536.1:c.4415T>C