Canonical Allele Identifier: PA2826566232
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142828
ClinVar RCV Id: RCV000132259 RCV000785297 RCV003237742 RCV002288655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg298Leu
CA000015
NM_001276760.3:c.893G>T