Canonical Allele Identifier: PA2499245356
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167722
ClinVar RCV Id: RCV001517306
ClinVar Variation Id: 2579713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Gly385Arg
CA10406062
NM_001282651.2:c.1153G>C
CA10406063
NM_001282651.2:c.1153G>A