Allele Registry

Canonical Allele Identifier: PA2828231737

Gene: DEAF1 HGNC NCBI

ClinVar RCV:

RCV000119805

ClinVar Variation:

133292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001354319.1:p.Gln22Pro	CA156397 NM_001367390.1:c.65A>C