Canonical Allele Identifier: PA2825606764
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148392
ClinVar RCV Id: RCV004440297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Phe109_Arg110del
CA645589280
NM_001126114.3:c.325_330del