Canonical Allele Identifier: PA2826567656
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1697592
ClinVar RCV Id: RCV002268876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Thr273Ile
CA397836069
NM_001276761.3:c.818C>T