Canonical Allele Identifier: PA2579977152
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1028584
ClinVar RCV Id: RCV001329663 RCV002464449 RCV002476541
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Met139Leu
CA4239635
NM_000162.5:c.415A>T
CA367402058
NM_000162.5:c.415A>C