Canonical Allele Identifier: PA658669091
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447423
ClinVar RCV Id: RCV000516528 RCV002463710 RCV002527475 RCV003325964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Gly296Ser
CA367400140
NM_033507.3:c.886G>A