Canonical Allele Identifier: PA2829108814
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373227.1:p.Ser1643Leu
CA158114
NM_001386298.1:c.4928C>T