Allele Registry

Canonical Allele Identifier: PA2827936439

Gene: GCK HGNC NCBI

ClinVar RCV:

RCV000431394

RCV000479407

RCV002402377

ClinVar Variation:

377026

418225

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341729.1:p.Met57Ile	CA16603236 NM_001354800.1:c.171G>T CA16618473 NM_001354800.1:c.171G>A CA367403315 NM_001354800.1:c.171G>C