Canonical Allele Identifier: PA2826220653
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000022940
ClinVar Variation:
30040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184149.1:p.Glu521Ala
CA128856
NM_001197220.2:c.1562A>C