Allele Registry

Canonical Allele Identifier: PA2499291168

Gene: L2HGDH HGNC NCBI

ClinVar RCV:

RCV001308236

ClinVar Variation:

1010586

HGVS (amino-acid)	Matching Registered Transcripts
NP_079160.1:p.Gly40Arg	CA389648743 NM_024884.3:c.118G>C