Canonical Allele Identifier: PA2826563585
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12366
ClinVar RCV Id: RCV000013163 RCV000013164 RCV000115738 RCV000254693 RCV000418930 RCV000424109 RCV000422097 RCV000424627 RCV000422733 RCV000424218 RCV000431361 RCV000434044 RCV000436207 RCV000441169 RCV000439513 RCV000440815 RCV000443907 RCV000463420 RCV000424833 RCV000428779 RCV000429822 RCV000419960 RCV000433409 RCV000435547 RCV000437210 RCV000423826 RCV000430161 RCV000440474 RCV000444851 RCV000444900 RCV000785345 RCV001358389 RCV001527484 RCV001257517 RCV001527470 RCV002476955 RCV003162246 RCV003466853 RCV003492292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Arg114His
CA000434
NM_001276698.3:c.341G>A