Canonical Allele Identifier: PA2580189438
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1727472
ClinVar RCV Id: RCV002325812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Glu933Lys
CA2320355
NM_001293307.2:c.2797G>A