Canonical Allele Identifier: PA916045427
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 538458
ClinVar RCV Id: RCV000647775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Gln1494Glu
CA1943859
NM_001365536.1:c.4480C>G