Canonical Allele Identifier: PA2741997353
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691828
ClinVar RCV Id: RCV003494025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gln39Leu
CA367403522
NM_033507.3:c.116A>T