Canonical Allele Identifier: PA2827936553
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36218
ClinVar RCV Id: RCV000029881 RCV000432293 RCV003993658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Phe150Ser
CA213784
NM_001354800.1:c.449T>C