Canonical Allele Identifier: PA2830123398
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36236
ClinVar RCV Id: RCV000029899 RCV002362597 RCV003318496
ClinVar Variation Id: 2691826
ClinVar RCV Id: RCV003494023
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met209Ile
CA213814
NM_033508.3:c.627G>T
CA367401294
NM_033508.3:c.627G>C
CA367401296
NM_033508.3:c.627G>A