Canonical Allele Identifier: PA100188
Gene: PDE4D HGNC NCBI
ClinVar Allele:
38992
ClinVar RCV:
RCV000022937
ClinVar Variation:
30037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001098101.1:p.Ser190Ala
CA128850
NM_001104631.2:c.568T>G