Canonical Allele Identifier: PA2829668999
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1727718
ClinVar RCV Id: RCV002326058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Glu1037Lys
CA2320349
NM_006514.4:c.3109G>A