Canonical Allele Identifier: PA2830122519
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2506148
ClinVar RCV Id: RCV003236379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val453Leu
CA367396891
NM_033507.3:c.1357G>C