Canonical Allele Identifier: PA2828042450
Gene: SLC35E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 3164397
ClinVar RCV Id: RCV004459285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341927.1:p.Ile35Val
CA6678257
NM_001354998.2:c.103A>G