Canonical Allele Identifier: PA2830124069
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 429500
ClinVar RCV Id: RCV000494422 RCV001290675 RCV002489206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Arg446Gln
CA367396940
NM_033508.3:c.1337G>A