Canonical Allele Identifier: PA2579982639
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3233991
ClinVar RCV Id: RCV004527567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ala449Ser
CA367396925
NM_000162.5:c.1345G>T