Canonical Allele Identifier: PA213789
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36221
ClinVar RCV Id: RCV000516927 RCV000991335 RCV002336092 RCV004527305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000153.1:p.Pro153Ser
CA213788
NM_000162.5:c.457C>T