ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579981110
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.129542209
Linked Data - NCBI & NCI
ClinVar Allele:
407150
ClinVar RCV:
RCV000480480
RCV000754804
RCV001731711
ClinVar Variation:
420070
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Gln38Pro
CA16618475
NM_000162.5:c.113A>C