Canonical Allele Identifier: PA916013606
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_001269576.1:p.Ser150Asn
CA10406070
NM_001282647.2:c.449G>A