Canonical Allele Identifier: PA2828151180
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30037
ClinVar RCV Id: RCV000022937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351529.1:p.Ser129Ala
CA128850
NM_001364600.2:c.385T>G