Canonical Allele Identifier: PA2828180365
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2938077
ClinVar RCV Id: RCV003796899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Glu420Gly
CA349085763
NM_001365536.1:c.1259A>G