Canonical Allele Identifier: PA645436402
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 328254
ClinVar RCV Id: RCV000392539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Arg929Cys
CA9225925
NM_000528.4:c.2785C>T