Canonical Allele Identifier: PA2826561609
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12368
ClinVar RCV Id: RCV000013167 RCV000420086 RCV000424688 RCV000429718 RCV000432461 RCV000434981 RCV000440816 RCV000428404 RCV000431210 RCV000432716 RCV000198779 RCV000441513 RCV000445307 RCV000422958 RCV000423074 RCV000437764 RCV000441912 RCV000418209 RCV000422446 RCV002433452 RCV004018618 RCV003332081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg241Thr
CA000445
NM_001276696.3:c.722G>C