Canonical Allele Identifier: PA2826562969
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376679
ClinVar RCV Id: RCV000421406 RCV000422095 RCV000424159 RCV000427021 RCV000426404 RCV000428833 RCV000431660 RCV000434430 RCV000437297 RCV000439053 RCV000439742 RCV000443298 RCV000443877 RCV000444003 RCV000633347 RCV002338982 RCV004022250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263627.1:p.Tyr4Asn
CA16603093
NM_001276698.3:c.10T>A