Canonical Allele Identifier: PA2826559686
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 482218
ClinVar RCV Id: RCV000564461 RCV000695145 RCV002289816
ClinVar Variation Id: 482235
ClinVar RCV Id: RCV000564049 RCV002289824 RCV000696578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Val164Leu
CA397840385
NM_001276695.3:c.490G>T
CA397840390
NM_001276695.3:c.490G>C