Canonical Allele Identifier: PA2827472730
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000022936
ClinVar Variation:
30036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336170.1:p.Phe155Ser
CA128848
NM_001349241.2:c.464T>C