Canonical Allele Identifier: PA916045302
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6364
ClinVar RCV Id: RCV000006736
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu869Phe
CA340554
NM_001365536.1:c.2605C>T