Canonical Allele Identifier: PA658740504
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 495051
ClinVar RCV Id: RCV000585701
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005205.2:p.Pro138Thr
CA350138742
NM_005214.5:c.412C>A