Canonical Allele Identifier: PA2825181776
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150130
ClinVar RCV Id: RCV003067415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.His94Arg
CA305478925
NM_000528.4:c.281A>G