Canonical Allele Identifier: PA915973572
Gene: PDE4D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098101.1:p.Glu651Ala
CA128856
NM_001104631.2:c.1952A>C