Canonical Allele Identifier: PA2827475363
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 2421466
ClinVar RCV Id: RCV003115767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336182.1:p.Arg222Cys
CA2322550
NM_001349253.2:c.664C>T