Canonical Allele Identifier: PA2826562529
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12364
ClinVar RCV Id: RCV000013161 RCV000148905 RCV000144670 RCV000236400 RCV000425909 RCV000432561 RCV000417906 RCV000420798 RCV000437607 RCV000422920 RCV000210145 RCV000426680 RCV000444544 RCV000433225 RCV000435581 RCV000441472 RCV000442231 RCV000444687 RCV000424430 RCV000722016 RCV000434706 RCV000785546 RCV000423580 RCV000430759 RCV000431084 RCV000436175 RCV001270278 RCV003315223
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Arg123Trp
CA000454
NM_001276697.3:c.367C>T
CA645588375
NM_001276697.3:c.366_367delinsTT