Canonical Allele Identifier: PA2826559954
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_001263624.1:p.Arg209Trp
CA000382
NM_001276695.3:c.625C>T
CA645373070
NM_001276695.3:c.624_625delinsTT