Canonical Allele Identifier: PA106902
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 215997
ClinVar RCV Id: RCV000197359 RCV000235315 RCV000434190 RCV000418175 RCV000435410 RCV000438333 RCV000424784 RCV000442329 RCV000433358 RCV000439892 RCV000427629 RCV000442357 RCV000443293 RCV000439245 RCV000422025 RCV000422663 RCV000423497 RCV000429197 RCV000568594 RCV000785533 RCV001610519 RCV002288809 RCV003320135 RCV003468892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Cys275Tyr
CA337141
NM_000546.6:c.824G>A