Canonical Allele Identifier: PA2826567749
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12379
ClinVar RCV Id: RCV000013178 RCV000128923 RCV000197240 RCV000413754 RCV000576817 RCV000481814 RCV000989700 RCV001375632 RCV002307364 RCV002496338 RCV003162248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg298His
CA000013
NM_001276761.3:c.893G>A