Canonical Allele Identifier: PA2825410777
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444804
ClinVar RCV Id: RCV000513019 RCV001511787
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035963.1:p.Ala347Thr
CA10406070
NM_001042498.3:c.1039G>A