Canonical Allele Identifier: PA2826560378
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 485040
ClinVar RCV Id: RCV000562780 RCV000822098 RCV002289833
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Asp2Asn
CA397847025
NM_001276696.3:c.4G>A