Canonical Allele Identifier: PA2830124082
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Ser452Leu
CA213760
NM_033508.3:c.1355C>T