Canonical Allele Identifier: PA2826832465
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 2139514
ClinVar RCV Id: RCV003052633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Gly491Val
CA352167765
NM_001293306.2:c.1472G>T