Allele Registry

Canonical Allele Identifier: PA2827281529

Gene: TP63 HGNC NCBI

ClinVar Allele:

21566

ClinVar RCV:

RCV000006900

RCV000394306

RCV000812084

RCV002283440

ClinVar Variation:

6527

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316893.1:p.Arg241Trp	CA118334 NM_001329964.2:c.721C>T