Canonical Allele Identifier: PA2826567465
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376656
ClinVar RCV Id: RCV000418085 RCV000420280 RCV000420482 RCV000422550 RCV000422795 RCV000424918 RCV000425669 RCV000427515 RCV000427884 RCV000431180 RCV000430119 RCV000431455 RCV000432372 RCV000435074 RCV000433489 RCV000435480 RCV000436543 RCV000438218 RCV000439774 RCV000440794 RCV000440997 RCV000444595 RCV000445287 RCV000445314 RCV000561782 RCV000698744 RCV002289535
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Arg234Ser
CA001542
NM_001276761.3:c.700C>A
CA645588417
NM_001276761.3:c.700_702delinsTCG
CA645588420
NM_001276761.3:c.699_700delinsAA