Canonical Allele Identifier: PA2825602774
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717844
ClinVar RCV Id: RCV002297843
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Gln38Arg
CA397847963
NM_001126113.3:c.113A>G