ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827937434
Gene: GCK
HGNC
NCBI
Linked Data
ClinVar Variation Id:
36200
ClinVar RCV Id:
RCV000517061
RCV000763582
RCV002271378
RCV002285258
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001341732.1:p.Ser131Leu
CA213760
NM_001354803.2:c.392C>T