Canonical Allele Identifier: PA2826559182
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142206
ClinVar RCV Id: RCV000131196 RCV000195648 RCV001356391 RCV001704056 RCV002267879 RCV002288646 RCV003149906
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg71Cys
CA000119
NM_001276695.3:c.211C>T
CA645589283
NM_001276695.3:c.210_211delinsTT