Canonical Allele Identifier: PA2827264920
Gene: TP63 HGNC NCBI

Linked Data

ClinVar Variation Id: 372540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316075.1:p.Ile397Thr
CA16042490
NM_001329146.2:c.1190T>C