Canonical Allele Identifier: PA101297
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_000519.2:p.Thr355Pro
CA351002
NM_000528.4:c.1063A>C