Canonical Allele Identifier: PA2830123397
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 16141
ClinVar RCV Id: RCV000017521 RCV000190348 RCV001281107 RCV003318493
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met209Lys
CA204367
NM_033508.3:c.626T>A