Canonical Allele Identifier: PA2741997497
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2503894
ClinVar RCV Id: RCV003230885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly171_Lys173dup
CA2573050986
NM_033507.3:c.512_520dup