Canonical Allele Identifier: PA916045394
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 130268
ClinVar RCV Id: RCV000118306 RCV001053070 RCV002354302
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Tyr1348Cys
CA231503
NM_001365536.1:c.4043A>G