Canonical Allele Identifier: PA2826832918
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1727718
ClinVar RCV Id: RCV002326058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Glu1036Lys
CA2320349
NM_001293306.2:c.3106G>A