Canonical Allele Identifier: PA2826567298
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 12349
ClinVar RCV Id: RCV000013142 RCV000161025 RCV000417593 RCV000426090 RCV000430002 RCV000419737 RCV000436186 RCV000440197 RCV000425471 RCV000441334 RCV000428895 RCV000492412 RCV000440886 RCV000418673 RCV000443435 RCV000423577 RCV000424262 RCV000436330 RCV000633397 RCV000434535 RCV001271056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly206Cys
CA000369
NM_001276761.3:c.616G>T