Canonical Allele Identifier: PA213795
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36225
ClinVar RCV Id: RCV000029888
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly170Val
CA213794
NM_000162.5:c.509G>T