Canonical Allele Identifier: PA2828151355
Gene: PDE4D HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351532.1:p.Glu349Ala
CA128856
NM_001364603.1:c.1046A>C