Canonical Allele Identifier: PA2826567747
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 177879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg298Pro
CA000014
NM_001276761.3:c.893G>C