Canonical Allele Identifier: PA2828816817
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2839214
ClinVar RCV Id: RCV003723349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366175.1:p.Thr276Ser
CA355916887
NM_001379246.1:c.826A>T
CA355916889
NM_001379246.1:c.827C>G