Canonical Allele Identifier: PA2826661689
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444804
ClinVar RCV Id: RCV000513019 RCV001511787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Ser126Asn
CA10406070
NM_001282648.2:c.377G>A