Canonical Allele Identifier: PA2826562017
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 216077
ClinVar RCV Id: RCV000198789 RCV000418938 RCV000423911 RCV000434089 RCV000421097 RCV000421751 RCV000439388 RCV000441624 RCV000434805 RCV000442071 RCV000429852 RCV000436603 RCV000438726 RCV000419621 RCV000428484 RCV000429211 RCV000437301 RCV000487386 RCV000785324 RCV001024600 RCV001271054 RCV002288812 RCV003474953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263626.1:p.Ile36Thr
CA002232
NM_001276697.3:c.107T>C