Allele Registry

Canonical Allele Identifier: PA2580403023

Gene: CHST11 HGNC NCBI

ClinVar RCV:

RCV004198092

ClinVar Variation:

2358221

HGVS (amino-acid)	Matching Registered Transcripts
NP_060883.1:p.Glu238Lys	CA6756650 NM_018413.6:c.712G>A