Canonical Allele Identifier: PA2827511920
Gene: PDE8B HGNC NCBI

Linked Data

ClinVar Variation Id: 354148
ClinVar RCV Id: RCV000344411 RCV004022002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336680.1:p.Arg94Gly
CA10620773
NM_001349751.3:c.280A>G