Canonical Allele Identifier: PA2827937181
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2734990
ClinVar RCV Id: RCV003555324
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341730.1:p.Val69Ala
CA367398363
NM_001354801.1:c.206T>C