Canonical Allele Identifier: PA2830122619
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393398
ClinVar RCV Id: RCV000445551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Leu24Gln
CA16609255
NM_033508.3:c.71T>A