Canonical Allele Identifier: PA2825608150
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376670
ClinVar Variation Id: 406596

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Val216Leu
CA16603084
NM_001126114.3:c.646G>T
CA16615950
NM_001126114.3:c.646G>C