Canonical Allele Identifier: PA2829669018
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2625775
ClinVar RCV Id: RCV003387221

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ser1053Tyr
CA2320335
NM_006514.4:c.3158C>A