Allele Registry

Canonical Allele Identifier: PA115602

Gene: XYLT2 HGNC NCBI

ClinVar RCV:

RCV000002642

RCV000989952

RCV001642196

RCV002276528

ClinVar Variation:

2533

HGVS (amino-acid)	Matching Registered Transcripts
NP_071450.2:p.Thr801Arg	CA115601 NM_022167.4:c.2402C>G