Canonical Allele Identifier: PA2826559998
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 420134
ClinVar RCV Id: RCV000483701 RCV000525682 RCV002289629 RCV002289630
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ile216del
CA16620619
NM_001276695.3:c.647_649del