Canonical Allele Identifier: PA2573088379
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 572450

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Gln556His
CA2320791
NM_006514.4:c.1668A>T
CA352167254
NM_006514.4:c.1668A>C