Canonical Allele Identifier: PA2499288970
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1056276
ClinVar RCV Id: RCV001365078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Asp646Asn
CA7927727
NM_022166.4:c.1936G>A