Canonical Allele Identifier: PA2828180377
Gene: SCN9A HGNC NCBI

Linked Data

ClinVar Variation Id: 498859
ClinVar RCV Id: RCV000591420 RCV000706997 RCV002384296
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352465.1:p.Arg429His
CA1944555
NM_001365536.1:c.1286G>A