Canonical Allele Identifier: PA2827937070
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36200
ClinVar RCV Id: RCV000517061 RCV000763582 RCV002271378 RCV002285258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Ser453Leu
CA213760
NM_001354800.1:c.1358C>T