Allele Registry

Canonical Allele Identifier: PA916045421

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000656133

RCV002527439

ClinVar Variation:

446178

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile1472Asn	CA349058419 NM_001365536.1:c.4415T>A