Canonical Allele Identifier: PA128859
Gene: PDE4D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159371.1:p.Gly612Asp
CA128858
NM_001165899.2:c.1835G>A