Canonical Allele Identifier: PA2826560770
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376563
ClinVar RCV Id: RCV000418158 RCV000420954 RCV000422074 RCV000423071 RCV000429525 RCV000428411 RCV000432330 RCV000433361 RCV000437581 RCV000438642 RCV000439732 RCV000445231 RCV000444598 RCV000570655 RCV000785515 RCV000991142 RCV004022201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Cys96Gly
CA16602989
NM_001276696.3:c.286T>G