Canonical Allele Identifier: PA2829668824
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3068525
ClinVar RCV Id: RCV003993716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ala499Asp
CA352167687
NM_006514.4:c.1496C>A