Canonical Allele Identifier: PA100129
Gene: PDE4D HGNC NCBI

Linked Data

ClinVar Variation Id: 40064
ClinVar RCV Id: RCV000033154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098101.1:p.Ala304Val
CA130730
NM_001104631.2:c.911C>T