Canonical Allele Identifier: PA2580451105
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2267318
ClinVar RCV Id: RCV002804001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Ala663Thr
CA395219391
NM_022166.4:c.1987G>A