Canonical Allele Identifier: PA2830122752
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 631495
ClinVar RCV Id: RCV000778070 RCV001816832 RCV002332563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.His49Tyr
CA367403394
NM_033508.3:c.145C>T