Canonical Allele Identifier: PA2579978047
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393398
ClinVar RCV Id: RCV000445551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Leu25Gln
CA16609255
NM_000162.5:c.74T>A