Canonical Allele Identifier: PA166912
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119585.1:p.Ala83Glu
CA000082
NM_001126113.3:c.248C>A