Canonical Allele Identifier: PA263413
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56094
ClinVar RCV Id: RCV000049503
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Ser132Trp
CA263411
NM_000170.3:c.395C>G