Canonical Allele Identifier: PA2826093379
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1007372
ClinVar RCV Id: RCV001304549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Ile595Asn
CA404244768
NM_001173498.2:c.1784T>A