Canonical Allele Identifier: PA2826560708
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 183748
ClinVar RCV Id: RCV000162461 RCV000237013 RCV000421040 RCV000417610 RCV000428519 RCV000426825 RCV000433024 RCV000441098 RCV000420028 RCV000457119 RCV000419372 RCV000421688 RCV000425628 RCV000430781 RCV000427448 RCV000431915 RCV000432405 RCV000436631 RCV000438666 RCV000438105 RCV000439150 RCV000442735 RCV000443535 RCV000576336 RCV003462117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Thr86Met
CA000140
NM_001276696.3:c.257C>T