Canonical Allele Identifier: PA2826559701
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376683
ClinVar RCV Id: RCV000418906 RCV000417872 RCV000423862 RCV000424176 RCV000428105 RCV000426347 RCV000428760 RCV000430958 RCV000433698 RCV000436591 RCV000435531 RCV000437249 RCV000438368 RCV000441249 RCV000440868 RCV000443239
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Tyr166Ser
CA16603097
NM_001276695.3:c.497A>C