Canonical Allele Identifier: PA2826560687
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 141098
ClinVar RCV Id: RCV000129457 RCV000213049 RCV000696142 RCV000785522 RCV004019730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Lys81Glu
CA000130
NM_001276696.3:c.241A>G