Canonical Allele Identifier: PA2580451110
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2142099
ClinVar RCV Id: RCV003058885 RCV003058886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg676Gln
CA7927700
NM_022166.4:c.2027G>A