Canonical Allele Identifier: PA2830122776
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1341600
ClinVar RCV Id: RCV001837096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Pro58Ala
CA367403309
NM_033508.3:c.172C>G