Canonical Allele Identifier: PA2827264226
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6528

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316073.1:p.Arg243Gln
CA118335
NM_001329144.2:c.728G>A