Canonical Allele Identifier: PA2830123388
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2691827
ClinVar RCV Id: RCV003494024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala207Pro
CA367401320
NM_033508.3:c.619G>C