Canonical Allele Identifier: PA2828548170
Gene: GCNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1182271
ClinVar RCV Id: RCV001539864 RCV003966162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361676.1:p.Thr102Ser
CA3631702
NM_001374747.1:c.305C>G
CA362707262
NM_001374747.1:c.304A>T