ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826562748
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
142828
ClinVar RCV Id:
RCV000132259
RCV000785297
RCV003237742
RCV002288655
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263626.1:p.Arg178Leu
CA000015
NM_001276697.3:c.533G>T