Canonical Allele Identifier: PA2826661721
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 697799
ClinVar RCV Id: RCV001485543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Gly162Arg
CA10406047
NM_001282648.2:c.484G>A
CA412893991
NM_001282648.2:c.484G>C