Canonical Allele Identifier: PA2828151477
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 101053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351533.1:p.Ile422Thr
CA150721
NM_001364604.1:c.1265T>C