Canonical Allele Identifier: PA2825075919
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 972774
ClinVar RCV Id: RCV001248984 RCV003481036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly68Asp
CA157919943
NM_000162.5:c.203G>A