Allele Registry

Canonical Allele Identifier: PA916045302

Gene: SCN9A HGNC NCBI

ClinVar RCV:

RCV000006736

ClinVar Variation:

6364

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Leu869Phe	CA340554 NM_001365536.1:c.2605C>T