ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579974867
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.479106022
Linked Data - NCBI & NCI
ClinVar Allele:
441110
ClinVar RCV:
RCV000516639
RCV001266633
RCV002463703
ClinVar Variation:
447410
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Val199Met
CA367401409
NM_000162.5:c.595G>A