Canonical Allele Identifier: PA2828816832
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 3027618
ClinVar RCV Id: RCV003890872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001366175.1:p.Phe291Ser
CA355917061
NM_001379246.1:c.872T>C