Canonical Allele Identifier: PA2827495935
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_001337084.1:p.Thr219Ser
CA355917549
NM_001350155.3:c.655A>T
CA355917556
NM_001350155.3:c.656C>G