Canonical Allele Identifier: PA2826562322
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12347
ClinVar Variation Id: 437017
ClinVar RCV Id: RCV000499534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg89Trp
CA000382
NM_001276697.3:c.265C>T
CA645373070
NM_001276697.3:c.264_265delinsTT