Canonical Allele Identifier: PA916006532
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 140786
ClinVar RCV Id: RCV000128936 RCV000235219 RCV000411273 RCV000588191 RCV000991146 RCV002498638 RCV003492581 RCV003917413
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Tyr68His
CA000104
NM_001276761.3:c.202T>C