Canonical Allele Identifier: PA2825139695
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 1919586
ClinVar RCV Id: RCV002630332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000274.3:p.Pro299Leu
CA2794165
NM_000283.4:c.896C>T