Canonical Allele Identifier: PA2827936431
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2097728
ClinVar RCV Id: RCV003018951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Thr49Ser
CA367403400
NM_001354800.1:c.146C>G
CA367403406
NM_001354800.1:c.145A>T