Canonical Allele Identifier: PA2579975965
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1341600
ClinVar RCV Id: RCV001837096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Pro59Ala
CA367403309
NM_000162.5:c.175C>G