ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579977073
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
1.615337584
Linked Data - NCBI & NCI
ClinVar RCV:
RCV001975403
RCV002052003
RCV003490980
ClinVar Variation:
1464253
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Met224Thr
CA367401149
NM_000162.5:c.671T>C