Canonical Allele Identifier: PA916045294
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 254095
ClinVar RCV Id: RCV000285786 RCV000384589 RCV000402179 RCV000498158 RCV001086993 RCV001332207 RCV000344215 RCV002450757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Val821Met
CA1944268
NM_001365536.1:c.2461G>A