Canonical Allele Identifier: PA2573171075
Gene: MAN2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516039
ClinVar RCV Id: RCV002023650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000519.2:p.Pro356Ala
CA404248745
NM_000528.4:c.1066C>G