Canonical Allele Identifier: PA2826662138
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 936005
ClinVar RCV Id: RCV001204715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269579.1:p.Pro384Leu
CA10406056
NM_001282650.2:c.1151C>T