Allele Registry

Canonical Allele Identifier: PA2573288987

Gene: L2HGDH HGNC NCBI

ClinVar RCV:

RCV001992090

ClinVar Variation:

1496852

HGVS (amino-acid)	Matching Registered Transcripts
NP_079160.1:p.Ala4Gly	CA7178148 NM_024884.3:c.11C>G