Canonical Allele Identifier: PA2826565902
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 233303
ClinVar RCV Id: RCV000220597 RCV000422798 RCV000422392 RCV000427379 RCV000428065 RCV000424659 RCV000429134 RCV000433685 RCV000434748 RCV000435298 RCV000439374 RCV000437591 RCV000444359 RCV000440058 RCV000417840 RCV000434911 RCV000423426 RCV000444283 RCV000445304 RCV001854689 RCV002288888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263689.1:p.Gly227Val
CA10580919
NM_001276760.3:c.680G>T