Canonical Allele Identifier: PA128857
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 30040
ClinVar RCV Id: RCV000022940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001159371.1:p.Glu590Ala
CA128856
NM_001165899.2:c.1769A>C