Canonical Allele Identifier: PA2828817229
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 438190
ClinVar RCV Id: RCV000504664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366176.1:p.Leu237Pro
CA355916145
NM_001379247.1:c.710T>C