Canonical Allele Identifier: PA2826559732
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 135359
ClinVar RCV Id: RCV000123099 RCV000122176 RCV000130072 RCV000144664 RCV000420459 RCV000420595 RCV000424188 RCV000430755 RCV000441015 RCV000420734 RCV000428223 RCV000430946 RCV000432016 RCV000436981 RCV000443346 RCV000444201 RCV000425846 RCV000427005 RCV000430601 RCV000438230 RCV000438582 RCV000419636 RCV000420908 RCV000422008 RCV000432438 RCV000437236 RCV000444077 RCV000626448 RCV001255672 RCV001798386 RCV003460862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg174Gln
CA000302
NM_001276695.3:c.521G>A