Canonical Allele Identifier: PA2825579663
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Arg266Gln
CA118348
NM_001114978.2:c.797G>A