Canonical Allele Identifier: PA2580229290
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1769650
ClinVar RCV Id: RCV002385433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Thr57Ser
CA367397077
NM_001354802.1:c.170C>G
CA367397082
NM_001354802.1:c.169A>T