Canonical Allele Identifier: PA2826561979
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 3148387
ClinVar RCV Id: RCV004440292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ala30_Leu35del
CA2825002604
NM_001276697.3:c.87_104del