Canonical Allele Identifier: PA213764
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36202
ClinVar RCV Id: RCV000029865 RCV000711768 RCV001162070 RCV001162072 RCV001162069 RCV002463596 RCV002496452 RCV001162071 RCV003325947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met462Ile
CA213763
NM_000162.5:c.1386G>T
CA4239371
NM_000162.5:c.1386G>A
CA367396755
NM_000162.5:c.1386G>C