Canonical Allele Identifier: PA2826559032
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Pro33Cys
CA000069
NM_001276695.3:c.97_98delinsTG