Canonical Allele Identifier: PA2826567419
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 161516
ClinVar RCV Id: RCV000149050 RCV000418979 RCV000255749 RCV000444063 RCV000418383 RCV000421625 RCV000430374 RCV000431935 RCV000492556 RCV000422957 RCV000423995 RCV000433054 RCV000434273 RCV000441726 RCV000444033 RCV000424505 RCV000429269 RCV000429720 RCV000436020 RCV000440516 RCV000445061 RCV000709403 RCV000785456 RCV002288661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Gly227Glu
CA000421
NM_001276761.3:c.680G>A