Allele Registry

Canonical Allele Identifier: PA2827265084

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000494181

ClinVar Variation:

430080

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316077.1:p.Gly173Val	CA355750729 NM_001329148.2:c.518G>T