Canonical Allele Identifier: PA2825139618
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 92769
ClinVar RCV Id: RCV000078556 RCV000488132 RCV000987384 RCV001151689
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000274.3:p.Tyr219His
CA145993
NM_000283.4:c.655T>C