Canonical Allele Identifier: PA916018826
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 576536

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Thr966Met
CA2320325
NM_001293307.2:c.2897C>T