Allele Registry

Canonical Allele Identifier: PA2826559358

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003484952

ClinVar Variation:

2687707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Gln105_Leu106delinsHisMet	CA2697552107 NM_001276695.3:c.315_316delinsCA