Canonical Allele Identifier: PA2826565532
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Arg163Leu
CA000291
NM_001276760.3:c.488G>T