Canonical Allele Identifier: PA2826832921
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1022653
ClinVar RCV Id: RCV001322592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Cys1038Tyr
CA2320347
NM_001293306.2:c.3113G>A