Canonical Allele Identifier: PA2827495067
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 1466663
ClinVar RCV Id: RCV001966130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337083.1:p.Arg273Trp
CA355916870
NM_001350154.3:c.817C>T