Canonical Allele Identifier: PA2579977073
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1464253
ClinVar RCV Id: RCV001975403 RCV002052003 RCV003490980
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met224Thr
CA367401149
NM_000162.5:c.671T>C