Canonical Allele Identifier: PA2827281750
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 372540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Ile574Thr
CA16042490
NM_001329964.2:c.1721T>C