Canonical Allele Identifier: PA2826561130
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 451799
ClinVar RCV Id: RCV000522967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gly160Val
CA397840476
NM_001276696.3:c.479G>T