Canonical Allele Identifier: PA2826561871
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428866
ClinVar RCV Id: RCV000492442 RCV000702915 RCV004023278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.His9Arg
CA287488569
NM_001276697.3:c.26A>G