Canonical Allele Identifier: PA167498
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Leu257Arg
CA000404
NM_001126113.3:c.770T>G