Canonical Allele Identifier: PA2830124036
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1769650
ClinVar RCV Id: RCV002385433
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Thr436Ser
CA367397077
NM_033508.3:c.1307C>G
CA367397082
NM_033508.3:c.1306A>T