Canonical Allele Identifier: PA1139693675
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 956333
ClinVar RCV Id: RCV001229116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Arg342His
CA329098725
NM_001282651.2:c.1025G>A