Canonical Allele Identifier: PA916039405
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36187
ClinVar RCV Id: RCV000029850 RCV001288976 RCV002345255 RCV003234925
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Arg81Gly
CA213737
NM_001354803.2:c.241C>G