ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579981669
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.059773828
Linked Data - NCBI & NCI
ClinVar RCV:
RCV003887333
ClinVar Variation:
3026940
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Asp198Ala
CA367401419
NM_000162.5:c.593A>C