ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579976367
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.232260472
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000516995
RCV004527383
ClinVar Variation:
447389
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Phe423Ser
CA367397256
NM_000162.5:c.1268T>C