Canonical Allele Identifier: PA2826567464
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376655
ClinVar RCV Id: RCV000418738 RCV000418536 RCV000421259 RCV000423633 RCV000423490 RCV000426132 RCV000423981 RCV000425890 RCV000428692 RCV000429444 RCV000427314 RCV000431067 RCV000433315 RCV000434296 RCV000434695 RCV000437048 RCV000436818 RCV000435767 RCV000438507 RCV000441792 RCV000442241 RCV000444109 RCV000444782 RCV000444989 RCV000515526 RCV000568814 RCV000785524 RCV000822080 RCV001539823 RCV002289534 RCV002502455
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg234Leu
CA001530
NM_001276761.3:c.701G>T