Canonical Allele Identifier: PA2579976954
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1700673
ClinVar RCV Id: RCV002285551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met41Arg
CA367403469
NM_000162.5:c.122T>G