Canonical Allele Identifier: PA2573279210
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1374204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Arg662Gln
CA7927714
NM_022166.4:c.1985G>A