Canonical Allele Identifier: PA2826564886
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1786573
ClinVar RCV Id: RCV002430538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro33Gly
CA2580095108
NM_001276760.3:c.97_98delinsGG