Canonical Allele Identifier: PA213813
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36234
ClinVar RCV Id: RCV000029897 RCV002463603 RCV002513252
ClinVar Variation Id: 1807283
ClinVar RCV Id: RCV002475240
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asp205Glu
CA213812
NM_000162.5:c.615C>G
CA367401342
NM_000162.5:c.615C>A