Canonical Allele Identifier: PA2741872571
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2935189
ClinVar RCV Id: RCV003790843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Thr870Ile
CA349077965
NM_001365536.1:c.2609C>T