Canonical Allele Identifier: PA2828548171
Gene: GCNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2401860
ClinVar RCV Id: RCV002759009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361676.1:p.Ala116Val
CA3631720
NM_001374747.1:c.347C>T