Canonical Allele Identifier: PA2579976939
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804838
ClinVar RCV Id: RCV000992040 RCV002464351
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met41Val
CA367403472
NM_000162.5:c.121A>G