Canonical Allele Identifier: PA1139684026
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 866150
ClinVar RCV Id: RCV001073937 RCV001862525
ClinVar Variation Id: 907108
ClinVar RCV Id: RCV001156709 RCV001156708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138763.2:p.Thr604Ser
CA355917549
NM_001145291.2:c.1810A>T
CA355917556
NM_001145291.2:c.1811C>G