Canonical Allele Identifier: PA2573088369
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 845838
ClinVar RCV Id: RCV001048985 RCV002393241
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Arg498Trp
CA2320834
NM_006514.4:c.1492C>T