ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825604404
Gene: TP53
HGNC
NCBI
Linked Data
ClinVar Variation Id:
231165
ClinVar RCV Id:
RCV000216410
RCV000418400
RCV000423798
RCV000427483
RCV000431695
RCV000443813
RCV000443927
RCV000419494
RCV000425092
RCV000429772
RCV000433800
RCV000435372
RCV000436292
RCV000426017
RCV000434064
RCV000440531
RCV000440866
RCV003114386
RCV004020663
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001119585.1:p.Arg196Pro
CA10580934
NM_001126113.3:c.587G>C