Canonical Allele Identifier: PA658679407
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482207
ClinVar RCV Id: RCV000568716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Asp281_Arg283del
CA658656537
NM_001126114.3:c.838_846del