Canonical Allele Identifier: PA2827265140
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 208163

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.His247Arg
CA339766
NM_001329148.2:c.740A>G