Canonical Allele Identifier: PA213805
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36230
ClinVar RCV Id: RCV000029893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ile19Met
CA213804
NM_000162.5:c.57C>G