Canonical Allele Identifier: PA2827937157
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Asn54Lys
CA367398630
NM_001354801.1:c.162C>G
CA367398633
NM_001354801.1:c.162C>A