Canonical Allele Identifier: PA916006338
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12354
ClinVar RCV Id: RCV000013148 RCV000129809 RCV000426292 RCV000430302 RCV000419614 RCV000424935 RCV000231770 RCV000432119 RCV000436867 RCV000442015 RCV000419041 RCV000436295 RCV000440992 RCV000785282 RCV000425602 RCV002247332 RCV003314552 RCV002288484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Cys83Tyr
CA000361
NM_001276699.3:c.248G>A