Canonical Allele Identifier: PA2825579635
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 161514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001108450.1:p.Arg226His
CA174179
NM_001114978.2:c.677G>A