Canonical Allele Identifier: PA2830123471
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2441736
ClinVar RCV Id: RCV003147994 RCV003147991 RCV003147992 RCV003147993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_277043.1:p.Asn230Ile
CA367400768
NM_033508.3:c.689A>T