Canonical Allele Identifier: PA1139735022
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 948833
ClinVar RCV Id: RCV001220168
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val1909Ile
CA349051639
NM_001365536.1:c.5725G>A