Canonical Allele Identifier: PA913199742
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 628970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119586.1:p.Arg290Gly
CA397836598
NM_001126114.3:c.868C>G