Canonical Allele Identifier: PA2826662132
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449924

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269579.1:p.Gln380Arg
CA10406058
NM_001282650.2:c.1139A>G