Canonical Allele Identifier: PA2826565586
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 231214
ClinVar RCV Id: RCV000220461 RCV000420213 RCV000424407 RCV000426111 RCV000429975 RCV000441598 RCV000419521 RCV000423147 RCV000418520 RCV000423776 RCV000441029 RCV000425014 RCV000443926 RCV000430230 RCV000430895 RCV000434458 RCV000435742 RCV000436779 RCV000431639 RCV000433848 RCV000443850 RCV000440212 RCV000440917 RCV000506128 RCV002288865 RCV002518297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg174Pro
CA10580932
NM_001276760.3:c.521G>C