Canonical Allele Identifier: PA2827265325
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.Ile545Thr
CA118342
NM_001329148.2:c.1634T>C