Canonical Allele Identifier: PA2826833386
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 418471
ClinVar RCV Id: RCV000578045 RCV000577983 RCV002341126 RCV001704586 RCV002496851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Val1616Phe
CA2319796
NM_001293306.2:c.4846G>T