Canonical Allele Identifier: PA2825606990
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 428902
ClinVar RCV Id: RCV000492742 RCV000821569 RCV002289677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Asn131Ile
CA397842926
NM_001126114.3:c.392A>T