Canonical Allele Identifier: PA164732
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141193
ClinVar RCV Id: RCV000129588
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Arg241_Arg244delinsHis
CA000443
NM_001126118.1:c.721_731delinsCA