Canonical Allele Identifier: PA2828151123
Gene: PDE4D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351528.1:p.Glu590Ala
CA128856
NM_001364599.1:c.1769A>C