Allele Registry

Canonical Allele Identifier: PA2827281479

Gene: TP63 HGNC NCBI

ClinVar RCV:

RCV002000613

ClinVar Variation:

1481716

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.Gly171Ser	CA355750726 NM_001329964.2:c.511G>A