Canonical Allele Identifier: PA2579975091
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1314557
ClinVar RCV Id: RCV001773066 RCV002463814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Trp167Gly
CA367401767
NM_000162.5:c.499T>G