Allele Registry

Canonical Allele Identifier: PA2828180495

Gene: SCN9A HGNC NCBI

ClinVar Allele:

283355

ClinVar RCV:

RCV000293514

RCV000346132

RCV000363472

RCV000401490

RCV000493503

RCV000688718

ClinVar Variation:

331988

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Arg540His	CA1944463 NM_001365536.1:c.1619G>A