Canonical Allele Identifier: PA1139748957
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 911631
ClinVar RCV Id: RCV001164187 RCV001164188 RCV001164189 RCV001164190 RCV001315293 RCV002468180 RCV003325990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Asp218Asn
CA4239564
NM_033507.3:c.652G>A