Canonical Allele Identifier: PA263368
Gene: GLDC HGNC NCBI

Linked Data

ClinVar Variation Id: 56075
ClinVar RCV Id: RCV000049484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.Arg790Trp
CA263366
NM_000170.3:c.2368C>T