Canonical Allele Identifier: PA100155
Gene: PDE4D HGNC NCBI
ClinVar RCV:
RCV000022941
ClinVar Variation:
30041
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098101.1:p.Gly673Asp
CA128858
NM_001104631.2:c.2018G>A