Canonical Allele Identifier: PA2827936907
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1802685
ClinVar RCV Id: RCV002465963 RCV003326018
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Val367Leu
CA367398995
NM_001354800.1:c.1099G>T
CA367398997
NM_001354800.1:c.1099G>C