Canonical Allele Identifier: PA100173
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30036
ClinVar RCV Id: RCV000022936
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098101.1:p.Phe226Ser
CA128848
NM_001104631.2:c.677T>C