Canonical Allele Identifier: PA2830123395
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2505485
ClinVar RCV Id: RCV003234753
ClinVar Variation Id: 2505486
ClinVar RCV Id: RCV003234754
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met209Val
CA367401305
NM_033508.3:c.625A>G
CA2018007653
NM_033508.3:c.624_625delinsAG