Allele Registry

Canonical Allele Identifier: PA2827281610

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV000006915

RCV000326964

ClinVar Variation:

6541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.Asp349Gly	CA118341 NM_001329964.2:c.1046A>G