Canonical Allele Identifier: PA2826561819
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 492635
ClinVar RCV Id: RCV000583939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263625.1:p.Gln294Glu
CA001088
NM_001276696.3:c.880C>G