Canonical Allele Identifier: PA2826563035
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182963
ClinVar RCV Id: RCV000161065 RCV000810785 RCV002288703
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg16Leu
CA000252
NM_001276698.3:c.47G>T