Canonical Allele Identifier: PA2825606779
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233627
ClinVar Variation Id: 641505
ClinVar RCV Id: RCV000794759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg110Pro
CA10580948
NM_001126114.3:c.329G>C
CA915949545
NM_001126114.3:c.329_330delinsCC