Canonical Allele Identifier: PA916013616
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 453301
ClinVar RCV Id: RCV000560194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269579.1:p.Cys95Phe
CA412897640
NM_001282650.2:c.284G>T