Canonical Allele Identifier: PA2826560170
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 486555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Arg244Pro
CA397836790
NM_001276695.3:c.731G>C