Canonical Allele Identifier: PA2827512072
Gene: PDE8B HGNC NCBI

Linked Data

ClinVar Variation Id: 6390
ClinVar RCV Id: RCV000006762

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336681.1:p.His203Pro
CA118185
NM_001349752.3:c.608A>C