Canonical Allele Identifier: PA2827495173
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 866150
ClinVar Variation Id: 907108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337083.1:p.Thr325Ser
CA355917549
NM_001350154.3:c.973A>T
CA355917556
NM_001350154.3:c.974C>G