Canonical Allele Identifier: PA2826566702
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500748
ClinVar RCV Id: RCV002015887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263690.1:p.Lys100Arg
CA397842677
NM_001276761.3:c.299A>G