Canonical Allele Identifier: PA2573171105
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491091
ClinVar RCV Id: RCV001986278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Gln505Arg
CA404246136
NM_000528.4:c.1514A>G