ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825618852
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
376585
ClinVar RCV Id:
RCV000419187
RCV000419880
RCV000421597
RCV000422382
RCV000422971
RCV000424398
RCV000427237
RCV000429763
RCV000431847
RCV000430133
RCV000432647
RCV000437480
RCV000438115
RCV000436876
RCV000440017
RCV000442319
RCV000442636
RCV000443331
RCV000792342
RCV004022209
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119590.1:p.Asp242Tyr
CA16603009
NM_001126118.1:c.724G>T