Canonical Allele Identifier: PA2826560649
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233627
ClinVar RCV Id: RCV000222678 RCV000231991 RCV002288889 RCV003462528
ClinVar Variation Id: 641505
ClinVar RCV Id: RCV000794759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Arg71Pro
CA10580948
NM_001276696.3:c.212G>C
CA915949545
NM_001276696.3:c.212_213delinsCC