Canonical Allele Identifier: PA2579975528
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1705456
ClinVar RCV Id: RCV002283770
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Tyr125Cys
CA367402194
NM_000162.5:c.374A>G