Canonical Allele Identifier: PA2826567787
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2039935
ClinVar RCV Id: RCV002886135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Ala308Phe
CA2580094845
NM_001276761.3:c.922_923delinsTT