Canonical Allele Identifier: PA2826559596
Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687701
ClinVar RCV Id: RCV003484946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263624.1:p.Asp145His
CA397841195
NM_001276695.3:c.433G>C