Canonical Allele Identifier: PA2827281736
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 373405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Cys559Tyr
CA16042469
NM_001329964.2:c.1676G>A