Canonical Allele Identifier: PA213815
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36236
ClinVar RCV Id: RCV000029899 RCV002362597 RCV003318496
ClinVar Variation Id: 2691826
ClinVar RCV Id: RCV003494023
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met210Ile
CA213814
NM_000162.5:c.630G>T
CA367401294
NM_000162.5:c.630G>C
CA367401296
NM_000162.5:c.630G>A