Canonical Allele Identifier: PA263378
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56079
ClinVar RCV Id: RCV000049488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Thr830Met
CA263376
NM_000170.3:c.2489C>T