Canonical Allele Identifier: PA2741997561
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2505485
ClinVar RCV Id: RCV003234753
ClinVar Variation Id: 2505486
ClinVar RCV Id: RCV003234754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Met211Val
CA367401305
NM_033507.3:c.631A>G
CA2018007653
NM_033507.3:c.630_631delinsAG