Canonical Allele Identifier: PA2499239897
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 13109
ClinVar Variation Id: 1068671
ClinVar RCV Id: RCV001380304

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138763.2:p.Trp807Arg
CA256723
NM_001145291.2:c.2419T>A
CA2795056
NM_001145291.2:c.2419T>C