Canonical Allele Identifier: PA645459490
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393398
ClinVar RCV Id: RCV000445551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Leu26Gln
CA16609255
NM_033507.3:c.77T>A