Canonical Allele Identifier: PA193827
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182969
ClinVar RCV Id: RCV000161073 RCV000468644 RCV000588363 RCV000663214 RCV002492643
ClinVar Variation Id: 186086
ClinVar RCV Id: RCV000165615 RCV002516487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119590.1:p.Gly295Arg
CA000006
NM_001126118.1:c.883G>A
CA000007
NM_001126118.1:c.883G>C