Canonical Allele Identifier: PA2741872605
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2933343
ClinVar RCV Id: RCV003790461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Tyr1037Cys
CA59791528
NM_001365536.1:c.3110A>G