Canonical Allele Identifier: PA2825410763
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1919471
ClinVar RCV Id: RCV002594837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035963.1:p.Asp321Gly
CA412894632
NM_001042498.3:c.962A>G