Canonical Allele Identifier: PA2829669026
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 3225644
ClinVar RCV Id: RCV004516926

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Glu1063Lys
CA2320327
NM_006514.4:c.3187G>A