Canonical Allele Identifier: PA2826566139
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Thr273Ser
CA000505
NM_001276760.3:c.818C>G
CA397836079
NM_001276760.3:c.817A>T