Canonical Allele Identifier: PA2830122239
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233998
ClinVar RCV Id: RCV004527574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val390Ala
CA367398657
NM_033507.3:c.1169T>C