Canonical Allele Identifier: PA263285
Gene: GLDC HGNC NCBI
ClinVar RCV:
RCV000049447
ClinVar Variation:
56038
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000161.2:p.His371Asp
CA263283
NM_000170.3:c.1111C>G