Canonical Allele Identifier: PA2826566103
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly263Glu
CA16615695
NM_001276760.3:c.788G>A