Canonical Allele Identifier: PA2826567664
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 185212
ClinVar RCV Id: RCV000164586 RCV000793553 RCV001255575 RCV003895130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ser276Thr
CA000506
NM_001276761.3:c.826T>A