Canonical Allele Identifier: PA2579982083
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2632567
ClinVar RCV Id: RCV003416862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Arg369Pro
CA367398967
NM_000162.5:c.1106G>C