Canonical Allele Identifier: PA2828816818
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 997843
ClinVar RCV Id: RCV001293402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366175.1:p.Tyr277Cys
CA2794629
NM_001379246.1:c.830A>G