Canonical Allele Identifier: PA2827936395
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679551
ClinVar RCV Id: RCV002227430
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met34Ile
CA367403583
NM_001354800.1:c.102G>T
CA367403585
NM_001354800.1:c.102G>C
CA367403586
NM_001354800.1:c.102G>A