Canonical Allele Identifier: PA2826832943
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1002406

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Ser1059Ala
CA2320331
NM_001293306.2:c.3175T>G