Canonical Allele Identifier: PA2741997598
Gene: GCK HGNC NCBI
ClinVar RCV:
RCV003494029
ClinVar Variation:
2691832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val227Leu
CA367401125
NM_033507.3:c.679G>C
CA367401128
NM_033507.3:c.679G>T