Canonical Allele Identifier: PA2826566790
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 406564
ClinVar RCV Id: RCV000492645 RCV000506226 RCV000473602 RCV002269272 RCV004022603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Thr116Asn
CA16615709
NM_001276761.3:c.347C>A