Canonical Allele Identifier: PA2827281596
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316893.1:p.Arg341Gln
CA118340
NM_001329964.2:c.1022G>A