Allele Registry

Canonical Allele Identifier: PA111719

Gene: TP63 HGNC NCBI

ClinVar Allele:

21571

ClinVar RCV:

RCV000006905

RCV001280776

RCV002512857

RCV003162215

ClinVar Variation:

6532

HGVS (amino-acid)	Matching Registered Transcripts
NP_003713.3:p.Arg319Cys	CA118338 NM_003722.5:c.955C>T