Canonical Allele Identifier: PA2826565146
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376629
ClinVar RCV Id: RCV000418504 RCV000418722 RCV000421596 RCV000424301 RCV000428123 RCV000426255 RCV000426873 RCV000428765 RCV000431846 RCV000433916 RCV000434568 RCV000437107 RCV000439874 RCV000438364 RCV000441135 RCV000442900 RCV000546420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Lys93Met
CA16603048
NM_001276760.3:c.278A>T