Canonical Allele Identifier: PA2825610494
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376688
ClinVar RCV Id: RCV000419702 RCV000424584 RCV000423767 RCV000426310 RCV000429130 RCV000427847 RCV000429300 RCV000432093 RCV000434035 RCV000434427 RCV000437403 RCV000438679 RCV000438838 RCV000439357 RCV000443812 RCV001313857 RCV001575028 RCV000419021 RCV000419523 RCV000421037 RCV004022254 RCV000438068 RCV000570507
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119587.1:p.Tyr88Asn
CA16603101
NM_001126115.1:c.262T>A