Canonical Allele Identifier: PA2826220776
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30041
ClinVar RCV Id: RCV000022941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184150.1:p.Gly371Asp
CA128858
NM_001197221.2:c.1112G>A