Canonical Allele Identifier: PA213799
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36227
ClinVar RCV Id: RCV000029890 RCV002463599
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly178Arg
CA213798
NM_000162.5:c.532G>A
CA367401653
NM_000162.5:c.532G>C