Canonical Allele Identifier: PA2827937350
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2698504
ClinVar RCV Id: RCV003551796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341731.1:p.Ser53_Thr57del
CA2697557239
NM_001354802.1:c.157_171del