Canonical Allele Identifier: PA2827937288
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 981653
ClinVar RCV Id: RCV001261199 RCV002463795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Met13Thr
CA367398600
NM_001354802.1:c.38T>C