Canonical Allele Identifier: PA2825042339
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447397
ClinVar RCV Id: RCV000516818 RCV003993667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp124His
CA367402212
NM_000162.5:c.370G>C