Canonical Allele Identifier: PA172455
Gene: L2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 158799
ClinVar RCV Id: RCV000146250 RCV000676578 RCV001516293
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079160.1:p.Leu18Arg
CA172454
NM_024884.3:c.53T>G