Allele Registry

Canonical Allele Identifier: PA2826567452

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421804

RCV000422825

RCV000423493

RCV000424786

RCV000427639

RCV000429369

RCV000433521

RCV000434183

RCV000438331

RCV000440060

RCV000442761

RCV000442953

RCV000444340

RCV001228585

RCV004022247

ClinVar Variation:

376673

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263690.1:p.Val233Glu	CA16603087 NM_001276761.3:c.698T>A