Canonical Allele Identifier: PA2826559444
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 528248
ClinVar RCV Id: RCV000633348 RCV001091169 RCV002289922 RCV002289923
ClinVar Variation Id: 568285
ClinVar RCV Id: RCV001022965 RCV000688595 RCV002289962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg119Leu
CA397842028
NM_001276695.3:c.356G>T
CA645589033
NM_001276695.3:c.356_357delinsTT