Canonical Allele Identifier: PA2826562701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 630832
ClinVar RCV Id: RCV000776836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Asp165Tyr
CA397835843
NM_001276697.3:c.493G>T