Canonical Allele Identifier: PA2826561158
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376681
ClinVar RCV Id: RCV000422077 RCV000422980 RCV000427034 RCV000424901 RCV000427749 RCV000430410 RCV000431652 RCV000433236 RCV000432320 RCV000437968 RCV000437254 RCV000439980 RCV000440667 RCV000442863 RCV000443687 RCV000443828 RCV000704312 RCV002356520 RCV004022251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Tyr166Cys
CA16603095
NM_001276696.3:c.497A>G