Canonical Allele Identifier: PA2825612524
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_001119588.1:p.Gly22Asp
CA002547
NM_001126116.1:c.65G>A
CA2697552101
NM_001126116.1:c.65_66delinsAT