Allele Registry

Canonical Allele Identifier: PA2826220980

Gene: PDE4D HGNC NCBI

ClinVar RCV:

RCV000022938

ClinVar Variation:

30038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001184152.1:p.Thr296Pro	CA128852 NM_001197223.2:c.886A>C