Canonical Allele Identifier: PA2827936852
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 393397
ClinVar RCV Id: RCV000445474
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Leu307Phe
CA16609241
NM_001354800.1:c.918_919delinsAT
CA367400025
NM_001354800.1:c.919C>T