ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA213720
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.005069778
Linked Data - NCBI & NCI
ClinVar RCV:
RCV002281721
ClinVar Variation:
36178
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Met381Arg
CA213719
NM_000162.5:c.1142T>G