Canonical Allele Identifier: PA916030211
Gene: PDE8B HGNC NCBI

Linked Data

ClinVar Variation Id: 6390
ClinVar RCV Id: RCV000006762
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336678.1:p.His326Pro
CA118185
NM_001349749.3:c.977A>C