Canonical Allele Identifier: PA2825580277
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 6548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108452.1:p.Arg243Gly
CA340600
NM_001114980.1:c.727C>G