Canonical Allele Identifier: PA2825181747
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717060
ClinVar RCV Id: RCV002296242

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Gly76Asp
CA404258111
NM_000528.4:c.227G>A