Canonical Allele Identifier: PA2827265138
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 478110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316077.1:p.His247Tyr
CA355753773
NM_001329148.2:c.739C>T