ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA096528
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.549047074
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000029906
RCV000255932
RCV000825615
RCV002477021
RCV003155042
ClinVar Variation:
36243
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Val226Met
CA213827
NM_000162.5:c.676G>A