Canonical Allele Identifier: PA2828831519
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366409.1:p.Ser1643Leu
CA158114
NM_001379480.1:c.4928C>T