Canonical Allele Identifier: PA111644
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_003710.1:p.His305Pro
CA118185
NM_003719.5:c.914A>C