Canonical Allele Identifier: PA2827936669
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_001341729.1:p.Met210Ile
CA213814
NM_001354800.1:c.630G>T
CA367401294
NM_001354800.1:c.630G>C
CA367401296
NM_001354800.1:c.630G>A