Allele Registry

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Canonical Allele Identifier: PA645436064

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 237950

ClinVar RCV Id: RCV000231149 RCV000492535 RCV000662397 RCV001558177 RCV003332150 RCV002478839 RCV003469152

ClinVar Variation Id: 2687710

ClinVar RCV Id: RCV003484955

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119589.1:p.Gly22Asp	CA002547 NM_001126117.1:c.65G>A CA2697552101 NM_001126117.1:c.65_66delinsAT