Canonical Allele Identifier: PA645396434
Gene: GCNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 354701
ClinVar RCV Id: RCV000283024 RCV001483687 RCV003902375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001482.1:p.Pro85Arg
CA3631968
NM_001491.3:c.254C>G