Canonical Allele Identifier: PA2825076341
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2503894
ClinVar RCV Id: RCV003230885

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Gly170_Lys172dup
CA2573050986
NM_000162.5:c.509_517dup