Canonical Allele Identifier: PA263408
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56091
ClinVar RCV Id: RCV000049500
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Arg966Gly
CA263406
NM_000170.3:c.2896A>G