Canonical Allele Identifier: PA2830122498
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1505418
ClinVar RCV Id: RCV002004046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Ser446Arg
CA367396957
NM_033507.3:c.1338T>G
CA367396958
NM_033507.3:c.1338T>A
CA367396973
NM_033507.3:c.1336A>C