Canonical Allele Identifier: PA2826559900
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376663
ClinVar RCV Id: RCV000418625 RCV000419713 RCV000420813 RCV000421131 RCV000423572 RCV000424972 RCV000425344 RCV000426095 RCV000430014 RCV000430987 RCV000432092 RCV000431755 RCV000436296 RCV000437363 RCV000438864 RCV000440216 RCV000441902 RCV000441261 RCV000441922 RCV000785454 RCV001053974 RCV001576591 RCV002289538 RCV002289539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Ser202Tyr
CA16603078
NM_001276695.3:c.605C>A