Canonical Allele Identifier: PA2826565547
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376685
ClinVar RCV Id: RCV000419308 RCV000420368 RCV000421826 RCV000422887 RCV000424493 RCV000427755 RCV000426781 RCV000431739 RCV000431958 RCV000432726 RCV000437451 RCV000437587 RCV000439923 RCV000440094 RCV000443622 RCV000443753 RCV000819983 RCV000775886 RCV004022252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Tyr166His
CA16603099
NM_001276760.3:c.496T>C