ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA213718
Gene: GCK
HGNC
NCBI
Linked Data
ClinVar Variation Id:
36177
ClinVar RCV Id:
RCV000029840
RCV001642240
RCV003318495
RCV002444444
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Ala379Glu
CA213717
NM_000162.5:c.1136C>A