Canonical Allele Identifier: PA2825605469
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376644
ClinVar RCV Id: RCV000420956 RCV000424036 RCV000423863 RCV000425930 RCV000426582 RCV000431661 RCV000431945 RCV000431305 RCV000432244 RCV000441126 RCV000443337 RCV000444083 RCV000443990 RCV000572417 RCV000681956 RCV000785498 RCV000797363 RCV002289530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Pro278Arg
CA16603061
NM_001126113.3:c.833C>G