Canonical Allele Identifier: PA2830122121
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972776
ClinVar RCV Id: RCV001248986 RCV001879746 RCV003325991
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala379Gly
CA367398802
NM_033507.3:c.1136C>G