Canonical Allele Identifier: PA2573088366
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 948476

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ala493Thr
CA2320840
NM_006514.4:c.1477G>A