Allele Registry

Canonical Allele Identifier: PA2826220633

Gene: PDE4D HGNC NCBI

ClinVar RCV:

RCV000022938

ClinVar Variation:

30038

HGVS (amino-acid)	Matching Registered Transcripts
NP_001184149.1:p.Thr457Pro	CA128852 NM_001197220.2:c.1369A>C