Canonical Allele Identifier: PA2826092957
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 208282
ClinVar RCV Id: RCV000206997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Thr354Pro
CA351002
NM_001173498.2:c.1060A>C