Canonical Allele Identifier: PA111760
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6534

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.Arg343Gln
CA118340
NM_003722.5:c.1028G>A