Allele Registry

Canonical Allele Identifier: PA2826096023

Gene: CHST11 HGNC NCBI

ClinVar RCV:

RCV004198092

ClinVar Variation:

2358221

HGVS (amino-acid)	Matching Registered Transcripts
NP_001167453.1:p.Glu233Lys	CA6756650 NM_001173982.2:c.697G>A