Canonical Allele Identifier: PA2580345971
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1776227
ClinVar RCV Id: RCV002398744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Gly535Arg
CA352167422
NM_006514.4:c.1603G>C