Canonical Allele Identifier: PA2826567158
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161397

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro183Leu
CA000317
NM_001276761.3:c.548C>T
CA645588718
NM_001276761.3:c.547_548delinsTT