Canonical Allele Identifier: PA916039379
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 129140
ClinVar RCV Id: RCV000117127 RCV003325949 RCV003556165
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341732.1:p.Cys49Phe
CA152950
NM_001354803.2:c.146G>T