Canonical Allele Identifier: PA164731
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_001119589.1:p.Arg148_Arg151delinsHis
CA000443
NM_001126117.1:c.442_452delinsCA