Canonical Allele Identifier: PA2830122642
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1679551
ClinVar RCV Id: RCV002227430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met33Ile
CA367403583
NM_033508.3:c.99G>T
CA367403585
NM_033508.3:c.99G>C
CA367403586
NM_033508.3:c.99G>A