Canonical Allele Identifier: PA2826559678
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1061739
ClinVar RCV Id: RCV001371377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Asn161Asp
CA397840468
NM_001276695.3:c.481A>G