Canonical Allele Identifier: PA1139735281
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435297
ClinVar RCV Id: RCV000502957 RCV002287417
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala74dup
CA645372837
NM_001354802.1:c.221_223dup