Canonical Allele Identifier: PA100968
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1687
ClinVar RCV Id: RCV000001755 RCV000622985 RCV001091771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Arg750Trp
CA339901
NM_000528.4:c.2248C>T