Canonical Allele Identifier: PA2826562928
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485050
ClinVar RCV Id: RCV000569933 RCV001035792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Thr228Arg
CA287485465
NM_001276697.3:c.683C>G