Canonical Allele Identifier: PA2741997572
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691835
ClinVar RCV Id: RCV003494032 RCV003565693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Cys221Phe
CA367401193
NM_033507.3:c.662G>T