Canonical Allele Identifier: PA2826565710
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Tyr197Ser
CA000346
NM_001276760.3:c.590A>C