Allele Registry

Canonical Allele Identifier: PA2826561941

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376607

ClinVar RCV Id: RCV000419975 RCV000420594 RCV000421045 RCV000421558 RCV000423857 RCV000425641 RCV000425896 RCV000428479 RCV000431364 RCV000429821 RCV000431267 RCV000436580 RCV000437195 RCV000436952 RCV000439103 RCV000441082 RCV000444017 RCV000444951 RCV000444976 RCV000815181 RCV001293868 RCV002264935 RCV002289527

ClinVar Variation Id: 406578

ClinVar RCV Id: RCV000464573 RCV000567952 RCV001527472 RCV003159559

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.His20Gln	CA16603028 NM_001276697.3:c.60T>G CA16615708 NM_001276697.3:c.60T>A