Allele Registry

Canonical Allele Identifier: PA2825579601

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV002000613

ClinVar Variation:

1481716

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108450.1:p.Gly173Ser	CA355750726 NM_001114978.2:c.517G>A