Canonical Allele Identifier: PA2499253492
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1056690
ClinVar RCV Id: RCV001365557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val877Ile
CA1944229
NM_001365536.1:c.2629G>A