Canonical Allele Identifier: PA2580158059
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150130
ClinVar RCV Id: RCV003067415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.His94Arg
CA305478925
NM_001173498.2:c.281A>G