Canonical Allele Identifier: PA2826563625
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376644
ClinVar RCV Id: RCV000420956 RCV000424036 RCV000423863 RCV000425930 RCV000426582 RCV000431661 RCV000431945 RCV000431305 RCV000432244 RCV000441126 RCV000443337 RCV000444083 RCV000443990 RCV000572417 RCV000681956 RCV000785498 RCV000797363 RCV002289530
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Pro119Arg
CA16603061
NM_001276698.3:c.356C>G