Canonical Allele Identifier: PA2827936426
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 424481
ClinVar RCV Id: RCV000479996 RCV002285338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Arg46Met
CA16618474
NM_001354800.1:c.137G>T