Canonical Allele Identifier: PA156369
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 133282
ClinVar RCV Id: RCV000119795 RCV002514608 RCV004019663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119584.1:p.Thr150_Pro153del
CA000194
NM_001126112.3:c.448_459del