Canonical Allele Identifier: PA2829669034
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 259996
ClinVar RCV Id: RCV000249220 RCV001807172 RCV001513526 RCV002321929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Val1073Ala
CA2320322
NM_006514.4:c.3218T>C