Canonical Allele Identifier: PA2741853364
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2621908
ClinVar RCV Id: RCV004363681

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Asp943Glu
CA352156782
NM_001293307.2:c.2829C>G
CA352156783
NM_001293307.2:c.2829C>A