Canonical Allele Identifier: PA2827936439
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 377026
ClinVar RCV Id: RCV000431394
ClinVar Variation Id: 418225
ClinVar RCV Id: RCV000479407 RCV002402377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met57Ile
CA16603236
NM_001354800.1:c.171G>T
CA16618473
NM_001354800.1:c.171G>A
CA367403315
NM_001354800.1:c.171G>C