Canonical Allele Identifier: PA2826563244
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376661
ClinVar RCV Id: RCV000421044 RCV000422178 RCV000425174 RCV000431745 RCV000432876 RCV000437603 RCV000439391 RCV000442610 RCV000442691 RCV000465501 RCV000662560 RCV000785463 RCV002289537
ClinVar Variation Id: 428895
ClinVar RCV Id: RCV000492567 RCV004023282 RCV002523445
ClinVar Variation Id: 2020649
ClinVar RCV Id: RCV002857438
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Ser56Arg
CA16603076
NM_001276698.3:c.168T>G
CA397839990
NM_001276698.3:c.168T>A
CA397840019
NM_001276698.3:c.166A>C