Canonical Allele Identifier: PA645509826
Gene: SLC35D1 HGNC NCBI

Linked Data

ClinVar Variation Id: 440280
ClinVar RCV Id: RCV000507444 RCV000727150 RCV001078524 RCV002279293 RCV002524926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055954.1:p.Ala272Thr
CA898862
NM_015139.3:c.814G>A