Canonical Allele Identifier: PA100774
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161114
ClinVar RCV Id: RCV000148295 RCV001311981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005205.2:p.Arg70Trp
CA173999
NM_005214.5:c.208C>T