Canonical Allele Identifier: PA2827936648
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 198050
ClinVar RCV Id: RCV000711778 RCV002272161 RCV002354464 RCV003883139
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ala201Ser
CA246541
NM_001354800.1:c.601G>T