Canonical Allele Identifier: PA2579975201
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2097728
ClinVar RCV Id: RCV003018951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Thr49Ser
CA367403400
NM_000162.5:c.146C>G
CA367403406
NM_000162.5:c.145A>T