Canonical Allele Identifier: PA2826565666
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Cys190Arg
CA16620623
NM_001276760.3:c.568T>C