Canonical Allele Identifier: PA2573088576
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Leu577His
CA16611281
NM_006514.4:c.1730T>A