Canonical Allele Identifier: PA2825381056
Gene: CTLA4 HGNC NCBI

Linked Data

ClinVar Variation Id: 495051
ClinVar RCV Id: RCV000585701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001032720.1:p.Pro138Thr
CA350138742
NM_001037631.3:c.412C>A