Canonical Allele Identifier: PA2826559742
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376616
ClinVar RCV Id: RCV000421427 RCV000423188 RCV000427039 RCV000427702 RCV000431675 RCV000433885 RCV000437948 RCV000440391 RCV000442701 RCV000445284 RCV000444957 RCV002298583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.His175Leu
CA16603036
NM_001276695.3:c.524A>T