Allele Registry

Canonical Allele Identifier: PA339768

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000206266

RCV000312203

RCV000821003

ClinVar Variation:

208163

HGVS (amino-acid)	Matching Registered Transcripts
NP_003713.3:p.His247Arg	CA339766 NM_003722.5:c.740A>G