Canonical Allele Identifier: PA168217
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 142386
ClinVar RCV Id: RCV000131474 RCV000553568 RCV000986048 RCV001192621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000537.3:p.Val73Met
CA000075
NM_000546.6:c.217G>A