Canonical Allele Identifier: PA2826220236
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000022936
ClinVar Variation:
30036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001184147.1:p.Phe162Ser
CA128848
NM_001197218.2:c.485T>C