Canonical Allele Identifier: PA2827495770
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 438190
ClinVar RCV Id: RCV000504664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337084.1:p.Leu131Pro
CA355916145
NM_001350155.3:c.392T>C