Canonical Allele Identifier: PA2579981849
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 435299
ClinVar RCV Id: RCV000502737 RCV002463691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Asn391Lys
CA367398630
NM_000162.5:c.1173C>G
CA367398633
NM_000162.5:c.1173C>A