Allele Registry

Canonical Allele Identifier: PA915993269

Gene: MAN2B1 HGNC NCBI

ClinVar RCV:

RCV000224033

RCV001080162

RCV001699242

ClinVar Variation:

235747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166969.1:p.Thr312Asn	CA9226650 NM_001173498.2:c.935C>A