Canonical Allele Identifier: PA166338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141762
ClinVar RCV Id: RCV000130396 RCV000422242 RCV000430048 RCV000437052 RCV000438381 RCV000439440 RCV000419337 RCV000421166 RCV000429447 RCV000431855 RCV000419825 RCV000423651 RCV000428748 RCV000444676 RCV000581322 RCV001069143 RCV004019738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119589.1:p.Cys3Tyr
CA000160
NM_001126117.1:c.8G>A