Canonical Allele Identifier: PA2826661905
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Gln306Arg
CA10406058
NM_001282649.2:c.917A>G