Allele Registry

Canonical Allele Identifier: PA2825579731

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000006915

RCV000326964

ClinVar Variation:

6541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001108450.1:p.Asp351Gly	CA118341 NM_001114978.2:c.1052A>G