Canonical Allele Identifier: PA1139683995
Gene: PDE6B HGNC NCBI

Linked Data

ClinVar Variation Id: 866660
ClinVar RCV Id: RCV001074863 RCV001206651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138763.2:p.Thr571Met
CA2794640
NM_001145291.2:c.1712C>T