ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826562276
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
12354
ClinVar RCV Id:
RCV000013148
RCV000129809
RCV000426292
RCV000430302
RCV000419614
RCV000424935
RCV000231770
RCV000432119
RCV000436867
RCV000442015
RCV000419041
RCV000436295
RCV000440992
RCV000785282
RCV000425602
RCV002247332
RCV003314552
RCV002288484
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001263626.1:p.Cys83Tyr
CA000361
NM_001276697.3:c.248G>A