Canonical Allele Identifier: PA645381466
Gene: L2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 435698
ClinVar RCV Id: RCV000503896 RCV000882412 RCV003942637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079160.1:p.Ile392Val
CA7177787
NM_024884.3:c.1174A>G