Canonical Allele Identifier: PA2579976782
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2443137
ClinVar RCV Id: RCV003151529

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Phe123Leu
CA367402213
NM_000162.5:c.369C>G
CA367402215
NM_000162.5:c.369C>A
CA367402221
NM_000162.5:c.367T>C