Canonical Allele Identifier: PA2741941342
Gene: SCN11A HGNC NCBI

Linked Data

ClinVar Variation Id: 2935086
ClinVar RCV Id: RCV003790740
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054858.2:p.Cys1774Arg
CA352159029
NM_014139.3:c.5320T>C