Canonical Allele Identifier: PA916052761
Gene: OPLAH HGNC NCBI

Linked Data

ClinVar Variation Id: 790907
ClinVar RCV Id: RCV000973779
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060040.1:p.Gln931Arg
CA4931328
NM_017570.5:c.2792A>G