Canonical Allele Identifier: PA2827936537
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1028584
ClinVar RCV Id: RCV001329663 RCV002464449 RCV002476541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341729.1:p.Met139Leu
CA4239635
NM_001354800.1:c.415A>T
CA367402058
NM_001354800.1:c.415A>C