Canonical Allele Identifier: PA2830123721
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585929
ClinVar RCV Id: RCV000711789 RCV001805831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Gly317Arg
CA367399913
NM_033508.3:c.949G>A
CA367399914
NM_033508.3:c.949G>C