Allele Registry

Canonical Allele Identifier: PA2827473429

Gene: PDE4D HGNC NCBI

ClinVar RCV:

RCV000022938

ClinVar Variation:

30038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336172.1:p.Thr331Pro	CA128852 NM_001349243.2:c.991A>C