Canonical Allele Identifier: PA2826566067
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Lys253Glu
CA397836557
NM_001276760.3:c.757A>G