Canonical Allele Identifier: PA916039389
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 804834
ClinVar RCV Id: RCV000992036 RCV003883165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Ala57Val
CA367398790
NM_001354803.2:c.170C>T