Canonical Allele Identifier: PA2829668995
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1727472
ClinVar RCV Id: RCV002325812
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006505.4:p.Glu1031Lys
CA2320355
NM_006514.4:c.3091G>A