Canonical Allele Identifier: PA1139756017
Gene: ROGDI HGNC NCBI

Linked Data

ClinVar Variation Id: 969753
ClinVar RCV Id: RCV001245171
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_078865.1:p.Ala220Thr
CA7882566
NM_024589.3:c.658G>A