Canonical Allele Identifier: PA2827936386
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393398
ClinVar RCV Id: RCV000445551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu25Gln
CA16609255
NM_001354800.1:c.74T>A