Canonical Allele Identifier: PA916013654
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 509462
ClinVar RCV Id: RCV000651310 RCV000606151 RCV003437306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Val388Ile
CA10406060
NM_001282651.2:c.1162G>A