Canonical Allele Identifier: PA2830124087
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068512
ClinVar RCV Id: RCV003993704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ala453Val
CA367396861
NM_033508.3:c.1358C>T