Allele Registry

Canonical Allele Identifier: PA2580451277

Gene: XYLT2 HGNC NCBI

ClinVar RCV:

RCV002785761

ClinVar Variation:

1985871

HGVS (amino-acid)	Matching Registered Transcripts
NP_071450.2:p.Thr801Ile	CA8646734 NM_022167.4:c.2402C>T