Canonical Allele Identifier: PA2827936505
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 423914
ClinVar RCV Id: RCV000479911 RCV002464016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala119Thr
CA16618471
NM_001354800.1:c.355G>A