Canonical Allele Identifier: PA2828180361
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 2926092
ClinVar RCV Id: RCV003786378
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Tyr405His
CA349085875
NM_001365536.1:c.1213T>C