Canonical Allele Identifier: PA2826562002
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182931
ClinVar RCV Id: RCV000161029 RCV001024490 RCV001371035 RCV002288689 RCV003462108
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Gln33Arg
CA000273
NM_001276697.3:c.98A>G