Canonical Allele Identifier: PA2828832114
Gene: CIC HGNC NCBI

Linked Data

ClinVar Variation Id: 133909
ClinVar RCV Id: RCV000120576

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366411.1:p.Tyr2071Ser
CA158136
NM_001379482.1:c.6212A>C