Allele Registry

Canonical Allele Identifier: PA169192

Gene: TP53 HGNC NCBI

ClinVar RCV:

RCV000132069

RCV001050775

RCV002288653

ClinVar Variation:

142702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.Thr304Ala	CA000493 NM_001126114.3:c.910A>G