Canonical Allele Identifier: PA169590
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142854
ClinVar RCV Id: RCV000132297 RCV000409340 RCV000473980 RCV000478624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro72Ala
CA000070
NM_001126113.3:c.214C>G