Canonical Allele Identifier: PA2830122767
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 377026
ClinVar RCV Id: RCV000431394
ClinVar Variation Id: 418225
ClinVar RCV Id: RCV000479407 RCV002402377
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met56Ile
CA16603236
NM_033508.3:c.168G>T
CA16618473
NM_033508.3:c.168G>A
CA367403315
NM_033508.3:c.168G>C