Canonical Allele Identifier: PA916045303
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 6349
ClinVar RCV Id: RCV000006721 RCV002512849
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Leu869His
CA340542
NM_001365536.1:c.2606T>A