Canonical Allele Identifier: PA2830123119
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36218
ClinVar RCV Id: RCV000029881 RCV000432293 RCV003993658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Phe149Ser
CA213784
NM_033508.3:c.446T>C