Canonical Allele Identifier: PA2826566066
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12378

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Lys253Ile
CA000469
NM_001276760.3:c.758A>T