Canonical Allele Identifier: PA2826564365
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 182938
ClinVar RCV Id: RCV000161038 RCV000213059 RCV000633381 RCV001527101 RCV003150958 RCV003467273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Arg123Leu
CA000456
NM_001276699.3:c.368G>T