Canonical Allele Identifier: PA916018827
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_001280236.2:p.Val975Ala
CA2320322
NM_001293307.2:c.2924T>C