Canonical Allele Identifier: PA2573088568
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407757

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Lys496Glu
CA2320837
NM_006514.4:c.1486A>G