Canonical Allele Identifier: PA2579979232
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 918070
ClinVar RCV Id: RCV001175327 RCV001556494
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly258Ser
CA367400589
NM_000162.5:c.772G>A