Canonical Allele Identifier: PA2826093969
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328254
ClinVar RCV Id: RCV000392539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Arg928Cys
CA9225925
NM_001173498.2:c.2782C>T