Canonical Allele Identifier: PA2573197570
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1359668
ClinVar RCV Id: RCV001904483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Pro947Arg
CA352156762
NM_001293307.2:c.2840C>G