Canonical Allele Identifier: PA2826565607
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376670
ClinVar Variation Id: 406596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Val177Leu
CA16603084
NM_001276760.3:c.529G>T
CA16615950
NM_001276760.3:c.529G>C