Canonical Allele Identifier: PA2826567775
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 956897
ClinVar RCV Id: RCV001229784 RCV002379878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Leu305Val
CA397832512
NM_001276761.3:c.913C>G