Allele Registry

Canonical Allele Identifier: PA2826563047

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV003509352

ClinVar Variation:

2747064

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Pro18_Arg22del	CA2697552087 NM_001276698.3:c.52_66del