Canonical Allele Identifier: PA2580490798
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136523
ClinVar RCV Id: RCV003037219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277042.1:p.Val201Leu
CA367401396
NM_033507.3:c.601G>T
CA367401397
NM_033507.3:c.601G>C