Canonical Allele Identifier: PA2827496344
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 349398
ClinVar RCV Id: RCV000323274 RCV000378001 RCV001520398
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337084.1:p.Arg436Trp
CA2795106
NM_001350155.3:c.1306C>T