Canonical Allele Identifier: PA2573171131
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1501960
ClinVar RCV Id: RCV002045053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Val689Met
CA9226205
NM_000528.4:c.2065G>A