Canonical Allele Identifier: PA2826832476
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_001280235.2:p.Ala499Asp
CA352167687
NM_001293306.2:c.1496C>A