Canonical Allele Identifier: PA2826561509
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 245777

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Leu226Pro
CA10584586
NM_001276696.3:c.677T>C
CA645588450
NM_001276696.3:c.677_678delinsCT