Canonical Allele Identifier: PA2826661616
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 507814
ClinVar RCV Id: RCV000611329 RCV000885007 RCV002063005 RCV002413706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269576.1:p.Arg158Cys
CA10406067
NM_001282647.2:c.472C>T