ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA213714
Gene: GCK
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.647660575
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000029838
RCV002463593
ClinVar Variation:
36175
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000153.1:p.Ser375Phe
CA213713
NM_000162.5:c.1124C>T