Canonical Allele Identifier: PA2827475563
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 426113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Leu396Pro
CA352168024
NM_001349253.2:c.1187T>C