Canonical Allele Identifier: PA130731
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 40064
ClinVar RCV Id: RCV000033154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159371.1:p.Ala243Val
CA130730
NM_001165899.2:c.728C>T