ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA213809
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.1646622
Linked Data - NCBI & NCI
ClinVar Allele:
44896
ClinVar RCV:
RCV000029895
RCV002463602
RCV003883123
ClinVar Variation:
36232
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Met202Val
CA213808
NM_000162.5:c.604A>G