Canonical Allele Identifier: PA2825886110
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 1919586
ClinVar RCV Id: RCV002630332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138764.2:p.Pro20Leu
CA2794165
NM_001145292.2:c.59C>T