Canonical Allele Identifier: PA2827936716
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2441736
ClinVar RCV Id: RCV003147994 RCV003147991 RCV003147992 RCV003147993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Asn231Ile
CA367400768
NM_001354800.1:c.692A>T