Canonical Allele Identifier: PA2741976515
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2529330
ClinVar RCV Id: RCV003280704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg662Trp
CA7927715
NM_022166.4:c.1984C>T