Allele Registry

Canonical Allele Identifier: PA169188

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000132069

RCV001050775

RCV002288653

ClinVar Variation:

142702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119590.1:p.Thr265Ala	CA000493 NM_001126118.1:c.793A>G