Canonical Allele Identifier: PA213809
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36232
ClinVar RCV Id: RCV000029895 RCV002463602 RCV003883123
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met202Val
CA213808
NM_000162.5:c.604A>G