Canonical Allele Identifier: PA2826562827
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 234059
ClinVar RCV Id: RCV000213405 RCV000471717 RCV000481680 RCV000781911 RCV001723809 RCV003919893
ClinVar Variation Id: 2774646
ClinVar RCV Id: RCV003585848
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Gly197Arg
CA000803
NM_001276697.3:c.589G>C
CA287485729
NM_001276697.3:c.589G>A