Canonical Allele Identifier: PA2573210933
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1349429
ClinVar RCV Id: RCV002046935
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Lys898Arg
CA349077783
NM_001365536.1:c.2693A>G