Canonical Allele Identifier: PA2826559249
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376667
ClinVar RCV Id: RCV000419385 RCV000419630 RCV000423812 RCV000424026 RCV000423368 RCV000424710 RCV000425385 RCV000429727 RCV000428977 RCV000430321 RCV000432131 RCV000434737 RCV000436286 RCV000436638 RCV000436088 RCV000440628 RCV000440402 RCV000442028 RCV000442755 RCV000442833 RCV000524926 RCV000492090 RCV002289540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Thr86Arg
CA16044089
NM_001276695.3:c.257C>G