Canonical Allele Identifier: PA2830123048
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16138
ClinVar RCV Id: RCV000017518 RCV002513078 RCV003147297 RCV003147298 RCV003147299
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser130Pro
CA126213
NM_033508.3:c.388T>C