Canonical Allele Identifier: PA2828832797
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366414.1:p.Ser734Leu
CA158114
NM_001379485.1:c.2201C>T