Canonical Allele Identifier: PA193032
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185814
ClinVar RCV Id: RCV000165304 RCV000425268 RCV000426406 RCV000434621 RCV000424351 RCV000424542 RCV000443052 RCV000434295 RCV000441086 RCV000418746 RCV000432177 RCV000436402 RCV000436602 RCV000443071 RCV000457645 RCV000785341 RCV001527085 RCV002243833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val272Met
CA000427
NM_000546.6:c.814G>A