Canonical Allele Identifier: PA2826561109
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376619
ClinVar RCV Id: RCV000421805 RCV000421312 RCV000422467 RCV000427622 RCV000426991 RCV000429226 RCV000431547 RCV000429901 RCV000432185 RCV000437865 RCV000437242 RCV000439461 RCV000440129 RCV000442296 RCV000442729 RCV000445057 RCV001184465 RCV004022221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Ile156Ser
CA16603039
NM_001276696.3:c.467T>G