Canonical Allele Identifier: PA158137
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133909
ClinVar RCV Id: RCV000120576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055940.3:p.Tyr1162Ser
CA158136
NM_015125.5:c.3485A>C