Canonical Allele Identifier: PA2826561514
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376605
ClinVar RCV Id: RCV000419323 RCV000420436 RCV000419956 RCV000421105 RCV000422610 RCV000426767 RCV000425613 RCV000426755 RCV000430688 RCV000431795 RCV000432420 RCV000431342 RCV000435860 RCV000437000 RCV000439845 RCV000439191 RCV000441587 RCV000444661 RCV000803659 RCV001027017 RCV002289526
ClinVar Variation Id: 458566
ClinVar RCV Id: RCV000528667 RCV000785497 RCV001027016 RCV002289744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gly227Arg
CA16603026
NM_001276696.3:c.679G>C
CA397837142
NM_001276696.3:c.679G>A
CA645588448
NM_001276696.3:c.678_679delinsAA