Canonical Allele Identifier: PA2826567139
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 826488

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Pro180Leu
CA397839907
NM_001276761.3:c.539C>T
CA645588728
NM_001276761.3:c.539_540delinsTT