Canonical Allele Identifier: PA2825609774
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_001119587.1:p.Thr23Asn
CA16615709
NM_001126115.1:c.68C>A