Canonical Allele Identifier: PA2826899079
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001291744.1:p.Ser1643Leu
CA158114
NM_001304815.2:c.4928C>T