Canonical Allele Identifier: PA2826567453
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233323
ClinVar RCV Id: RCV000220536 RCV000422297 RCV000421184 RCV000419845 RCV000420090 RCV000431226 RCV000441216 RCV000441467 RCV000427960 RCV000430105 RCV000421439 RCV000432569 RCV000439065 RCV000444129 RCV002515714 RCV004020685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Val233Gly
CA10580918
NM_001276761.3:c.698T>G