Canonical Allele Identifier: PA2828180542
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 408584
ClinVar RCV Id: RCV000456843 RCV002411460
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg597Gln
CA1944432
NM_001365536.1:c.1790G>A