Canonical Allele Identifier: PA2825181709
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 808457
ClinVar RCV Id: RCV000996766 RCV002549949 RCV002549950
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Pro60Leu
CA9226883
NM_000528.4:c.179C>T