Canonical Allele Identifier: PA2827265335
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 373405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Cys557Tyr
CA16042469
NM_001329148.2:c.1670G>A