Canonical Allele Identifier: PA2826561396
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 127822

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Met207Arg
CA000376
NM_001276696.3:c.620T>G