Canonical Allele Identifier: PA2826832512
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1776227
ClinVar RCV Id: RCV002398744
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Gly535Arg
CA352167422
NM_001293306.2:c.1603G>C