Canonical Allele Identifier: PA2499246849
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1002406
ClinVar RCV Id: RCV001298826 RCV001509211 RCV002322194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Ser962Ala
CA2320331
NM_001293307.2:c.2884T>G