Canonical Allele Identifier: PA2827281625
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 1294557

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg374His
CA2752347
NM_001329964.2:c.1121G>A