Canonical Allele Identifier: PA2573088380
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 579447

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ala578Val
CA72986331
NM_006514.4:c.1733C>T