Canonical Allele Identifier: PA263361
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56072
ClinVar RCV Id: RCV000049481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Gly771Arg
CA263359
NM_000170.3:c.2311G>A
CA372879991
NM_000170.3:c.2311G>C