Canonical Allele Identifier: PA2826564887
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182953
ClinVar RCV Id: RCV000161055 RCV000554325 RCV000587915 RCV003488410 RCV000410841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Pro33Cys
CA000069
NM_001276760.3:c.97_98delinsTG