Canonical Allele Identifier: PA1139749090
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 918070
ClinVar RCV Id: RCV001175327 RCV001556494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly259Ser
CA367400589
NM_033507.3:c.775G>A