Canonical Allele Identifier: PA2830124097
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36202
ClinVar RCV Id: RCV000029865 RCV000711768 RCV001162070 RCV001162072 RCV001162069 RCV002463596 RCV002496452 RCV001162071 RCV003325947
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Met461Ile
CA213763
NM_033508.3:c.1383G>T
CA4239371
NM_033508.3:c.1383G>A
CA367396755
NM_033508.3:c.1383G>C