Canonical Allele Identifier: PA2827937199
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1807286
ClinVar RCV Id: RCV002475243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Lys77Asn
CA367398236
NM_001354801.1:c.231G>T
CA367398238
NM_001354801.1:c.231G>C