Canonical Allele Identifier: PA2580189448
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1707802
ClinVar RCV Id: RCV002286963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Thr946Ile
CA2320344
NM_001293307.2:c.2837C>T