Canonical Allele Identifier: PA2826559853
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182966
ClinVar RCV Id: RCV000161069 RCV001373091 RCV002288705 RCV002288704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr197Ser
CA000346
NM_001276695.3:c.590A>C