Canonical Allele Identifier: PA2499270357
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035066
ClinVar RCV Id: RCV001337883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005205.2:p.Pro156Leu
CA2067119
NM_005214.5:c.467C>T