Allele Registry

Canonical Allele Identifier: PA2827264295

Gene: TP63 HGNC NCBI

ClinVar Variation Id: 279913

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316073.1:p.Arg343Trp	CA10602901 NM_001329144.2:c.1027C>T