Canonical Allele Identifier: PA2825077080
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met251Ile
CA367400628
NM_000162.5:c.753G>T
CA367400629
NM_000162.5:c.753G>A
CA367400630
NM_000162.5:c.753G>C