Canonical Allele Identifier: PA130412
Gene: OPLAH HGNC NCBI

Linked Data

ClinVar Variation Id: 39636
ClinVar RCV Id: RCV000032836 RCV003914892
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060040.1:p.Val1089Ile
CA130411
NM_017570.5:c.3265G>A