Canonical Allele Identifier: PA263450
Gene: GLDC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Leu296Arg
CA263448
NM_000170.3:c.887T>G