Canonical Allele Identifier: PA2579975221
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 997872
ClinVar RCV Id: RCV001293492 RCV002463808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr437Pro
CA367397086
NM_000162.5:c.1309A>C