Canonical Allele Identifier: PA2826562318
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376652
ClinVar RCV Id: RCV000417693 RCV000418362 RCV000420498 RCV000422668 RCV000423297 RCV000425782 RCV000424776 RCV000425100 RCV000425394 RCV000427544 RCV000427948 RCV000430735 RCV000432931 RCV000432207 RCV000433611 RCV000435353 RCV000435050 RCV000436038 RCV000437882 RCV000441010 RCV000441711 RCV000440334 RCV000444356 RCV000444519 RCV000444427 RCV000633396 RCV000626118 RCV001026425 RCV004022238
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg89Gly
CA16603069
NM_001276697.3:c.265C>G