Canonical Allele Identifier: PA1139691139
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 975739
ClinVar RCV Id: RCV001252564

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Glu120Lys
CA404256548
NM_001173498.2:c.358G>A