Canonical Allele Identifier: PA2825606004
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1790705
ClinVar RCV Id: RCV002459647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Pro8Arg
CA397849290
NM_001126114.3:c.23C>G