Allele Registry

Canonical Allele Identifier: PA2828180093

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000020515

ClinVar Variation:

21348

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Ile136Val	CA341942 NM_001365536.1:c.406A>G