Canonical Allele Identifier: PA2827937438
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068512
ClinVar RCV Id: RCV003993704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala132Val
CA367396861
NM_001354803.2:c.395C>T