Canonical Allele Identifier: PA2827496170
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 966627
ClinVar RCV Id: RCV001241353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001337084.1:p.Asp333Glu
CA355919661
NM_001350155.3:c.999C>A
CA355919662
NM_001350155.3:c.999C>G