Canonical Allele Identifier: PA2826832518
Gene: SCN10A HGNC NCBI

Linked Data

ClinVar Variation Id: 1176456
ClinVar RCV Id: RCV001531997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280235.2:p.Gly540Cys
CA352167378
NM_001293306.2:c.1618G>T