Canonical Allele Identifier: PA916064761
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 662990
ClinVar RCV Id: RCV000820763
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Glu664Lys
CA7927712
NM_022166.4:c.1990G>A