Canonical Allele Identifier: PA916018824
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 407759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Gly953Arg
CA2320339
NM_001293307.2:c.2857G>A
CA352156728
NM_001293307.2:c.2857G>C