Canonical Allele Identifier: PA916076801
Gene: GCNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 701963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_663630.2:p.Ala169Thr
CA3632232
NM_145655.3:c.505G>A