Canonical Allele Identifier: PA645435645
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376694
ClinVar RCV Id: RCV000421176 RCV000422301 RCV000426248 RCV000431852 RCV000432981 RCV000438025 RCV000444573 RCV000444665 RCV000443891 RCV000427088 RCV000439518 RCV000463978 RCV000566931 RCV002289545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Tyr236Asn
CA16040589
NM_001126114.3:c.706T>A