Canonical Allele Identifier: PA2499288972
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026953
ClinVar RCV Id: RCV001327483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg657His
CA7927718
NM_022166.4:c.1970G>A