Canonical Allele Identifier: PA2826220778
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 101053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184150.1:p.Ile376Thr
CA150721
NM_001197221.2:c.1127T>C