Allele Registry

Canonical Allele Identifier: PA100207

Gene: PDE4D HGNC NCBI

ClinVar RCV:

RCV000022938

ClinVar Variation:

30038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001098101.1:p.Thr587Pro	CA128852 NM_001104631.2:c.1759A>C