ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826563583
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
185814
ClinVar RCV Id:
RCV000165304
RCV000425268
RCV000426406
RCV000434621
RCV000424351
RCV000424542
RCV000443052
RCV000434295
RCV000441086
RCV000418746
RCV000432177
RCV000436402
RCV000436602
RCV000443071
RCV000457645
RCV000785341
RCV001527085
RCV002243833
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263627.1:p.Val113Met
CA000427
NM_001276698.3:c.337G>A