Canonical Allele Identifier: PA916050107
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 631495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.His51Tyr
CA367403394
NM_033507.3:c.151C>T