Canonical Allele Identifier: PA645418557
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 373449
ClinVar RCV Id: RCV000413146 RCV000888814 RCV002523958 RCV003932534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg141Trp
CA7928199
NM_022166.4:c.421C>T