Canonical Allele Identifier: PA2826093032
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2194190
ClinVar RCV Id: RCV002624272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166969.1:p.Gly389Ala
CA9226559
NM_001173498.2:c.1166G>C