Canonical Allele Identifier: PA2573279174
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1470773
ClinVar RCV Id: RCV001964346 RCV003264350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg557Cys
CA394875313
NM_022166.4:c.1669C>T