Canonical Allele Identifier: PA658663205
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 478110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003713.3:p.His247Tyr
CA355753773
NM_003722.5:c.739C>T