Canonical Allele Identifier: PA2826832932
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1728045
ClinVar RCV Id: RCV002320677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Ser1046Gly
CA352156751
NM_001293306.2:c.3136A>G