Canonical Allele Identifier: PA2579976519
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734985
ClinVar RCV Id: RCV003555319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Ser453Trp
CA367396875
NM_000162.5:c.1358C>G