Allele Registry

Canonical Allele Identifier: PA2826093699

Gene: MAN2B1 HGNC NCBI

ClinVar RCV:

RCV000020367

ClinVar Variation:

21210

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166969.1:p.Leu808Pro	CA341737 NM_001173498.2:c.2423T>C