Canonical Allele Identifier: PA2829669012
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1728045
ClinVar RCV Id: RCV002320677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Ser1047Gly
CA352156751
NM_006514.4:c.3139A>G