Canonical Allele Identifier: PA2827265489
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316078.1:p.His153Arg
CA339766
NM_001329149.2:c.458A>G