Canonical Allele Identifier: PA645435897
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 231060
ClinVar RCV Id: RCV000222860 RCV000434099 RCV000437116 RCV000437377 RCV000444938 RCV000419328 RCV000419898 RCV000420123 RCV000421059 RCV000429654 RCV000431744 RCV000431835 RCV000418732 RCV000419080 RCV000436356 RCV000439039 RCV000422030 RCV000426561 RCV000426712 RCV000427328 RCV000427811 RCV000429434 RCV000442511 RCV000439246 RCV000440313 RCV000553607 RCV000785460 RCV002288863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg273Pro
CA10580917
NM_001126114.3:c.818G>C