Canonical Allele Identifier: PA2580127684
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169178
ClinVar RCV Id: RCV003100551

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Gly485Val
CA9226431
NM_000528.4:c.1454G>T