Allele Registry

Canonical Allele Identifier: PA2825610682

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000420529

RCV000422293

RCV000424589

RCV000427086

RCV000429783

RCV000432913

RCV000435309

RCV000436968

RCV000437739

RCV000442354

RCV000442966

RCV000443369

RCV002509381

RCV002524697

RCV004022231

ClinVar Variation:

376636

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119587.1:p.Met105Lys	CA001811 NM_001126115.1:c.314T>A