Canonical Allele Identifier: PA916064739
Gene: XYLT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 784680
ClinVar RCV Id: RCV000966430
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071449.1:p.Gly640Ser
CA7927733
NM_022166.4:c.1918G>A