Canonical Allele Identifier: PA2826561935
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482223
ClinVar RCV Id: RCV000575494 RCV000633339 RCV002254704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His19Asp
CA397841387
NM_001276697.3:c.55C>G