Canonical Allele Identifier: PA2579974431
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1879689
ClinVar RCV Id: RCV002512334
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Val412Leu
CA367398284
NM_000162.5:c.1234G>T
CA367398286
NM_000162.5:c.1234G>C