Canonical Allele Identifier: PA2826564408
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 458572
ClinVar RCV Id: RCV000535005

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263628.1:p.Arg131Pro
CA397836589
NM_001276699.3:c.392G>C