Canonical Allele Identifier: PA2579977556
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 3068514
ClinVar RCV Id: RCV003993706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Lys143Asn
CA367402001
NM_000162.5:c.429G>T
CA367402002
NM_000162.5:c.429G>C