Canonical Allele Identifier: PA2826564465
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458574
ClinVar RCV Id: RCV000527123 RCV000561902 RCV000664300 RCV000986056 RCV000989706 RCV003330753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Arg147Gln
CA287486566
NM_001276699.3:c.440G>A