Allele Registry

Canonical Allele Identifier: PA2826563069

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV002037458

ClinVar Variation:

1345664

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.His20_Ser24del	CA2573154677 NM_001276698.3:c.58_72del