Allele Registry

Canonical Allele Identifier: PA2573288994

Gene: L2HGDH HGNC NCBI

ClinVar RCV:

RCV002029269

ClinVar Variation:

1514384

HGVS (amino-acid)	Matching Registered Transcripts
NP_079160.1:p.Gly39Arg	CA389648748 NM_024884.3:c.115G>C CA389648749 NM_024884.3:c.115G>A