Allele Registry

Canonical Allele Identifier: PA645435856

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376605

ClinVar RCV Id: RCV000419323 RCV000420436 RCV000419956 RCV000421105 RCV000422610 RCV000426767 RCV000425613 RCV000426755 RCV000430688 RCV000431795 RCV000432420 RCV000431342 RCV000435860 RCV000437000 RCV000439845 RCV000439191 RCV000441587 RCV000444661 RCV000803659 RCV001027017 RCV002289526

ClinVar Variation Id: 458566

ClinVar RCV Id: RCV000528667 RCV000785497 RCV001027016 RCV002289744

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.Gly266Arg	CA16603026 NM_001126114.3:c.796G>C CA397837142 NM_001126114.3:c.796G>A CA645588448 NM_001126114.3:c.795_796delinsAA