Allele Registry

Canonical Allele Identifier: PA2826562458

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12358

ClinVar RCV Id: RCV000013152 RCV000164988 RCV000427077 RCV000437706 RCV000443589 RCV001221969 RCV000420507 RCV000417682 RCV000426429 RCV000428361 RCV000431193 RCV000432989 RCV000434905 RCV000437100 RCV000439021 RCV000443570

ClinVar Variation Id: 574679

ClinVar RCV Id: RCV000696673 RCV002422533

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.Val113Leu	CA000430 NM_001276697.3:c.337G>T CA397837009 NM_001276697.3:c.337G>C