Canonical Allele Identifier: PA2827937355
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233991
ClinVar RCV Id: RCV004527567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ala69Ser
CA367396925
NM_001354802.1:c.205G>T