Canonical Allele Identifier: PA2826560705
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216465
ClinVar RCV Id: RCV000197507 RCV000421753 RCV000423507 RCV000438784 RCV000425663 RCV000427801 RCV000430716 RCV000433115 RCV000422366 RCV000436943 RCV000426240 RCV000430953 RCV000442723 RCV000443241 RCV000433745 RCV000443320 RCV000441651 RCV000420405 RCV000420607 RCV000431571 RCV000437594 RCV003165469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Thr86Lys
CA337257
NM_001276696.3:c.257C>A