Canonical Allele Identifier: PA2741872770
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2941331
ClinVar RCV Id: RCV003795033
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val1387Ala
CA349063375
NM_001365536.1:c.4160T>C