Canonical Allele Identifier: PA2828180368
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 1482373
ClinVar RCV Id: RCV002002914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu421Val
CA349085758
NM_001365536.1:c.1261T>G