Canonical Allele Identifier: PA2825886312
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2839214
ClinVar RCV Id: RCV003723349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138764.2:p.Thr276Ser
CA355916887
NM_001145292.2:c.826A>T
CA355916889
NM_001145292.2:c.827C>G