Canonical Allele Identifier: PA2741997557
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691827
ClinVar RCV Id: RCV003494024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ala209Pro
CA367401320
NM_033507.3:c.625G>C