Canonical Allele Identifier: PA2826566598
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 480734
ClinVar RCV Id: RCV000565147 RCV001322778 RCV002289783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala49Val
CA397845305
NM_001276761.3:c.146C>T