Canonical Allele Identifier: PA2499246848
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1022653
ClinVar RCV Id: RCV001322592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Cys941Tyr
CA2320347
NM_001293307.2:c.2822G>A