Canonical Allele Identifier: PA916045419
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6352
ClinVar RCV Id: RCV000006724
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Phe1460Val
CA340551
NM_001365536.1:c.4378T>G