Allele Registry

Canonical Allele Identifier: PA2826562959

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV001250514

RCV001361575

ClinVar Variation:

973858

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Ala2_Tyr4delinsAsp	CA915940817 NM_001276698.3:c.5_10del