Allele Registry

Canonical Allele Identifier: PA915993216

Gene: MAN2B1 HGNC NCBI

ClinVar RCV:

RCV000206959

RCV001572479

ClinVar Variation:

208251

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166969.1:p.Asp74Glu	CA350959 NM_001173498.2:c.222C>A CA404258148 NM_001173498.2:c.222C>G