Canonical Allele Identifier: PA2828151103
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000022938
ClinVar Variation:
30038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351528.1:p.Thr526Pro
CA128852
NM_001364599.1:c.1576A>C