Canonical Allele Identifier: PA213754
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36196
ClinVar RCV Id: RCV000029859 RCV001659731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly44Asp
CA213753
NM_000162.5:c.131G>A