Canonical Allele Identifier: PA2827264906
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 373405

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Cys382Tyr
CA16042469
NM_001329146.2:c.1145G>A