Canonical Allele Identifier: PA163659
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 140821
ClinVar RCV Id: RCV000129010 RCV000422367 RCV000435503 RCV000437895 RCV000440653 RCV000422134 RCV000422747 RCV000430047 RCV000437219 RCV000442540 RCV000419993 RCV000425179 RCV000430393 RCV000431764 RCV000432433 RCV000442627 RCV000419333 RCV000427647 RCV000440446 RCV000445294 RCV000785299 RCV001380073 RCV002288620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Arg243Gly
CA000453
NM_001126118.1:c.727C>G