Canonical Allele Identifier: PA2826565724
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182935
ClinVar RCV Id: RCV000161034 RCV000167907 RCV000235220 RCV000427976 RCV000439129 RCV000442204 RCV000442285 RCV000417749 RCV000418002 RCV000421991 RCV000420202 RCV000426546 RCV000426733 RCV000429110 RCV000433120 RCV000431283 RCV000436794 RCV000437851 RCV000438032 RCV000444562 RCV000785261 RCV001374444 RCV002288693 RCV003462109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Cys199Tyr
CA000351
NM_001276760.3:c.596G>A