Allele Registry

Canonical Allele Identifier: PA2826562005

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000164329

RCV000255425

RCV000417979

RCV000418086

RCV000418288

RCV000423052

RCV000423280

RCV000424475

RCV000425611

RCV000427767

RCV000428340

RCV000429618

RCV000433342

RCV000434391

RCV000434549

RCV000435651

RCV000435870

RCV000439433

RCV000439827

RCV000440903

RCV000445029

RCV000445148

RCV000460847

RCV000785346

RCV002288732

RCV003474857

ClinVar Variation:

184979

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.His34Arg	CA000274 NM_001276697.3:c.101A>G