ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579982680
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.5289664
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000518241
RCV003318500
ClinVar Variation:
447382
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Ala379Gly
CA367398793
NM_000162.5:c.1136C>G