Canonical Allele Identifier: PA2580222220
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1801903
ClinVar RCV Id: RCV002464722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Glu705Lys
CA349080740
NM_001365536.1:c.2113G>A