Canonical Allele Identifier: PA2826559468
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 422295
ClinVar RCV Id: RCV000481512 RCV000552464 RCV004023170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ala122Asp
CA16620630
NM_001276695.3:c.365C>A