Canonical Allele Identifier: PA915991032
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 809143
ClinVar RCV Id: RCV000997648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005205.2:p.Thr182Arg
CA350139056
NM_005214.5:c.545C>G