Canonical Allele Identifier: PA2827936685
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_001341729.1:p.Asp217Asn
CA4239564
NM_001354800.1:c.649G>A