Canonical Allele Identifier: PA891855213
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 585930
ClinVar RCV Id: RCV000711790 RCV002285408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val34Ala
CA367403604
NM_033507.3:c.101T>C