Allele Registry

Canonical Allele Identifier: PA2828180471

Gene: SCN9A HGNC NCBI

Linked Data

ClinVar RCV:

RCV000277449

RCV000290806

RCV000348148

RCV000388718

RCV000468717

RCV000723961

RCV000781948

RCV001332206

RCV002399622

ClinVar Variation:

193859

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001352465.1:p.Glu519Lys	CA239538 NM_001365536.1:c.1555G>A