Canonical Allele Identifier: PA2827937237
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1770532
ClinVar RCV Id: RCV002387880 RCV003774278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Ala113Ser
CA367396909
NM_001354801.1:c.337G>T