Canonical Allele Identifier: PA2826561086
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127816
ClinVar RCV Id: RCV000122174 RCV000205751 RCV000219468 RCV000662561 RCV000766937
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Pro152Arg
CA000272
NM_001276696.3:c.455C>G