Canonical Allele Identifier: PA2580189464
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1922182
ClinVar RCV Id: RCV002613601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280236.2:p.Pro961Leu
CA352156678
NM_001293307.2:c.2882C>T