Canonical Allele Identifier: PA2826562019
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376617
ClinVar RCV Id: RCV000417891 RCV000418677 RCV000420717 RCV000425266 RCV000423573 RCV000428137 RCV000426094 RCV000426791 RCV000430955 RCV000433525 RCV000433861 RCV000435534 RCV000436319 RCV000438337 RCV000441219 RCV000444892 RCV001270271 RCV001345722 RCV002356515 RCV003329275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ile36Phe
CA16603037
NM_001276697.3:c.106A>T