Allele Registry

Canonical Allele Identifier: PA915993249

Gene: MAN2B1 HGNC NCBI

ClinVar RCV:

RCV000207009

ClinVar Variation:

208257

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166969.1:p.Arg202Pro	CA351019 NM_001173498.2:c.605G>C