Canonical Allele Identifier: PA916045268
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 30357
ClinVar RCV Id: RCV000118297 RCV000191125 RCV000393721 RCV000476046 RCV000023302 RCV001546748 RCV002415425 RCV000311897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Ile731Lys
CA129149
NM_001365536.1:c.2192T>A