Canonical Allele Identifier: PA2828816839
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 418401
ClinVar RCV Id: RCV000479658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366175.1:p.Gly297Ser
CA2794667
NM_001379246.1:c.889G>A