Canonical Allele Identifier: PA2826661878
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1042432
ClinVar RCV Id: RCV001346389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Val270del
CA2428428820
NM_001282649.2:c.808_810del