Canonical Allele Identifier: PA645460248
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 381599
ClinVar RCV Id: RCV000419860
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met236Val
CA16605219
NM_033507.3:c.706A>G