Allele Registry

Canonical Allele Identifier: PA2826559528

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000417683

RCV000421780

RCV000423312

RCV000427345

RCV000427493

RCV000428483

RCV000429213

RCV000432458

RCV000433209

RCV000434691

RCV000438383

RCV000439916

RCV000440549

RCV000442009

RCV000443390

RCV000694763

RCV000785539

RCV001821147

RCV002289541

RCV002289542

RCV002596262

RCV004069069

ClinVar Variation:

376668

2185665

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263624.1:p.Val134Leu	CA16603082 NM_001276695.3:c.400G>T CA397841537 NM_001276695.3:c.400G>C CA3047147254 NM_001276695.3:c.399_400delinsGT