Allele Registry

Canonical Allele Identifier: PA2827937126

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV002281721

ClinVar Variation:

36178

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341730.1:p.Met44Arg	CA213719 NM_001354801.1:c.131T>G