Canonical Allele Identifier: PA2826564389
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 183752
ClinVar RCV Id: RCV000162466 RCV000255724 RCV000420427 RCV000422231 RCV000424388 RCV000431629 RCV000426778 RCV000437639 RCV000419251 RCV000421987 RCV000427820 RCV000431848 RCV000432936 RCV000506006 RCV000437453 RCV000439250 RCV000443333 RCV000443492 RCV000466372 RCV002288710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Glu127Lys
CA000464
NM_001276699.3:c.379G>A
CA645588351
NM_001276699.3:c.378_379delinsAA