Allele Registry

Canonical Allele Identifier: PA130412

Gene: OPLAH HGNC NCBI

ClinVar RCV:

RCV000032836

RCV003914892

ClinVar Variation:

39636

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