Canonical Allele Identifier: PA2827936541
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068514
ClinVar RCV Id: RCV003993706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Lys143Asn
CA367402001
NM_001354800.1:c.429G>T
CA367402002
NM_001354800.1:c.429G>C