Canonical Allele Identifier: PA150722
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 101053
ClinVar RCV Id: RCV000087311 RCV001854509
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159371.1:p.Ile617Thr
CA150721
NM_001165899.2:c.1850T>C