ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579977057
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.349248769
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000419860
ClinVar Variation:
381599
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Met235Val
CA16605219
NM_000162.5:c.703A>G