ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579977335
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.062274202
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000516508
RCV003330318
RCV003688859
ClinVar Variation:
447383
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Met381Lys
CA367398767
NM_000162.5:c.1142T>A