Allele Registry

Canonical Allele Identifier: PA2826561031

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV002037458

ClinVar Variation:

1345664

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.His140_Ser144del	CA2573154677 NM_001276696.3:c.418_432del