Canonical Allele Identifier: PA2579978794
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 631495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.His50Tyr
CA367403394
NM_000162.5:c.148C>T