Canonical Allele Identifier: PA2828640258
Gene: PDE8B HGNC NCBI

Linked Data

ClinVar Variation Id: 6390
ClinVar RCV Id: RCV000006762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362991.1:p.His204Pro
CA118185
NM_001376062.1:c.611A>C