Canonical Allele Identifier: PA2826220581
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 40064
ClinVar RCV Id: RCV000033154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184149.1:p.Ala174Val
CA130730
NM_001197220.2:c.521C>T