Allele Registry

Canonical Allele Identifier: PA100942

Gene: MAN2B1 HGNC NCBI

ClinVar RCV:

RCV000207009

ClinVar Variation:

208257

HGVS (amino-acid)	Matching Registered Transcripts
NP_000519.2:p.Arg202Pro	CA351019 NM_000528.4:c.605G>C